CDK1
Normalized values from positional scanning peptide array
Phospho-serine (pS) is a duplicate of phospho-tyrosine (pT) in PSPA
Position-wise Probabilities
Log-Odds: Probabilities / STY Background
Sites with acceptor types representing >8% and count ≥10 are included
S Sites Probabilities
T Sites Probabilities
Log-Odds: S Sites / S Background
Log-Odds: T Sites / T Background
Sites with acceptor types representing >8% and count ≥10 are included
Motif clusters with count ≥ 10 are shown
Download
| substrate_uniprot | site | source | substrate_genes | site_seq |
|---|---|---|---|---|
| A0A2R8Y4L2 | S6 | Sugiyama | HNRNPA1L3 HNRNPA1P48 | _______________MSKSEsPKEPEQLRKLFIGGLsFEtT |
| A6NKT7 | S1276 | EPSD|PSP | RGPD3 RGP3 | EDALDDsVssssVHAsPLAssPVRKNLFHFDESTTGSNFSF |
| O00115 | S70 | Sugiyama | DNASE2 DNASE2A DNL2 | QYKyLDEssGGWRDGRALINsPEGAVGRSLQPLyRSNTSQL |
| O00151 | S130 | Sugiyama | PDLIM1 CLIM1 CLP36 | PQEVLHIGsAHNRsAMPFtAsPAsSTTARVItNQyNNPAGL |
| O00267 | S666 | EPSD|PSP | SUPT5H SPT5 SPT5H | AGGSKPRDVtNFtVGGFAPMsPRIssPMHPSAGGQRGGFGs |
| O00267 | T806 | Sugiyama | SUPT5H SPT5 SPT5H | MYGsQtPLQDGsRtPHyGsQtPLHDGsRtPAQsGAWDPNNP |
| O00311 | T376 | SIGNOR|EPSD|PSP | CDC7 CDC7L1 | TDKVCSICLSRRQQVAPRAGtPGFRAPEVLTKCPNQTTAID |
| O00399 | T186 | SIGNOR|EPSD|PSP | DCTN6 WS3 | FLMKILPNYHHLKKTMKGSStPVKN________________ |
| O00418 | S359 | GPS6|SIGNOR|EPSD|PSP | EEF2K | NTKLLQSAKtILRGtEEKCGsPQVRTLsGSRPPLLRPLsEN |
| O00429 | S126 | Sugiyama | DNM1L DLP1 DRP1 | EIRQEIENETERISGNNKGVsPEPIHLKIFSPNVVNLTLVD |
| O00429 | S616 | GPS6|EPSD|PSP | DNM1L DLP1 DRP1 | SKAEELLAEEKsKPIPIMPAsPQKGHAVNLLDVPVPVARKL |
| O00443 | S259 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | PIK3C2A | NGKARTDLEITDSKVSNLQVsPKSEDISKFDWLDLDPLSKP |
| O00443 | S60 | Sugiyama | PIK3C2A | AKLQKDRQVTDNQRGFELsssTRKKAQVyNKQDyDLMVFPE |
| O00512 | T172 | PSP | BCL9 | RsstPsHGQttATEPTPAQKtPAKVVYVFSTEMANKAAEAV |
| O00562 | S382 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | PITPNM1 DRES9 NIR2 PITPNM | EVFPKEMtKWNsNDFIDAFAsPVEAEGtPEPGAEAAKGIED |
| O00562 | T287 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | PITPNM1 DRES9 NIR2 PITPNM | EAQPPGKPSTEARSAASNTGtPDGPEAPPGPDAsPDAsFGK |
| O00571 | T204 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | DDX3X DBX DDX3 | DVEMGEIIMGNIELTRYTRPtPVQKHAIPIIKEKRDLMACA |
| O00571 | T323 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | DDX3X DBX DDX3 | GADIGQQIRDLERGCHLLVAtPGRLVDMMERGKIGLDFCKy |
| O14497 | S363 | Sugiyama | ARID1A BAF250 BAF250A C1orf4 OSA1 SMARCF1 | AAAAAAASGGAQQRsHHAPMsPGssGGGGQPLARtPQPssP |
| O14545 | S327 | Sugiyama | TRAFD1 FLN29 | DHQTSCNPSRALPsLNtGsssPRGVEEPDVIFQNFLQQAAS |
| O14715 | S1275 | EPSD|PSP | RGPD8 RANBP2ALPHA RANBP2L1 RANBP2L3 | EDALDDsVssssVHAsPLAssPVRKNLFRFDESTTGSNFsF |
| O14745 | S280 | EPSD|PSP|Sugiyama | NHERF1 NHERF SLC9A3R1 | tNGEIQKENsREALAEAALEsPRPALVRsAssDtsEELNsQ |
| O14745 | S302 | EPSD|PSP | NHERF1 NHERF SLC9A3R1 | RPALVRsAssDtsEELNsQDsPPKQDSTAPSSTSSSDPILD |
| O14746 | T249 | SIGNOR|PSP | TERT EST2 TCS1 TRT | SRSLPLPKRPRRGAAPEPERtPVGQGSWAHPGRTRGPSDRG |
| O14757 | S286 | GPS6|SIGNOR|EPSD|PSP | CHEK1 CHK1 | NKPLKKGAKRPRVtsGGVsEsPsGFsKHIQsNLDFsPVNsA |
| O14757 | S301 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CHEK1 CHK1 | GGVsEsPsGFsKHIQsNLDFsPVNsAssEENVKYsssQPEP |
| O14773 | T201 | EPSD|PSP | TPP1 CLN2 GIG1 UNQ267/PRO304 | SLRQRPEPQVTGTVGLHLGVtPSVIRKRYNLTSQDVGSGTS |
| O14777 | T31 | PSP | NDC80 HEC HEC1 KNTC2 | AGRLsMQELRSQDVNKQGLYtPQTKEKPTFGKLsINKPtsE |
| O14974 | S473 | GPS6|EPSD | PPP1R12A MBS MYPT1 | tASKEGQKEKDTAGVTRsAssPRLsssLDNKEKEKDSKGTR |
| O14980 | S391 | EPSD|PSP | XPO1 CRM1 | EYWNHLAAELYREsPFstsAsPLLsGsQHFDVPPRRQLYLP |
| O14994 | S470 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | SYN3 | PQRSGsPsQQRLsPQGQQPLsPQsGsPQQQRSPGsPQLSRA |
| O15151 | S96 | SIGNOR|EPSD|PSP | MDM4 MDMX | CGGDLLGELLGRQSFSVKDPsPLyDMLRKNLVTLATATTDA |
| O15287 | S387 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | FANCG XRCC9 | YLDLLALLLDSSEPRFsPPPsPPGPCMPEVFLEAAVALIQA |
| O15297 | S40 | SIGNOR | PPM1D WIP1 | YMEDVTQIVVEPEPtAEEKPsPRRSLSQPLPPRPsPAALPG |
| O15350 | T86 | SIGNOR|EPSD|PSP | TP73 P73 | NLLSSTMDQMSSRAASASPYtPEHAASVPTHSPyAQPSSTF |
| O15392 | T34 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | BIRC5 API4 IAP4 | LKDHRIstFKNWPFLEGCACtPERMAEAGFIHCPtENEPDL |
| O15446 | S285 | EPSD|PSP | POLR1G ASE1 CAST CD3EAP PAF49 | EDKTVKQEQINTEPLEDtVLsPtKKRKRQKGTEGMEPEEGV |
| O15530 | T354 | EPSD|PSP | PDPK1 PDK1 | GPLKAHPFFESVTWENLHQQtPPKLTAYLPAMSEDDEDCyG |
| O43148 | T77 | SIGNOR|EPSD|PSP | RNMT KIAA0398 | RKRKEFEDDLVKEsssCGKDtPsKKRKLDPEIVPEEKDCGD |
| O43237 | S194 | Sugiyama | DYNC1LI2 DNCLI2 LIC2 | ERKFVKDFQDyMEPEEGCQGsPQRRGPLtsGsDEENVALPL |
| O43521 | S104 | SIGNOR | BCL2L11 BIM | RRSsLLSRsssGYFsFDTDRsPAPMSCDKSTQtPsPPCQAF |
| O43583 | S73 | PSP | DENR DRP1 H14 | CRQWLEKNFPNEFAKLtVENsPKQEAGIsEGQGtAGEEEEK |
| O43583 | T69 | PSP | DENR DRP1 H14 | DVAKCRQWLEKNFPNEFAKLtVENsPKQEAGIsEGQGtAGE |
| O43663 | T470 | GPS6|EPSD | PRC1 | RQLKNKKQTEtEMLyGsAPRtPsKRRGLAPNtPGKARKLNT |
| O43663 | T481 | GPS6|EPSD|PSP | PRC1 | EMLyGsAPRtPsKRRGLAPNtPGKARKLNTttMsNAtANss |
| O43683 | S593 | EPSD|PSP | BUB1 BUB1L | EEFLDDSTVWGIRCNKtLAPsPKsPGDFtsAAQLAstPFHK |
| O43683 | T609 | GPS6|SIGNOR|iPTMNet|EPSD|PSP | BUB1 BUB1L | tLAPsPKsPGDFtsAAQLAstPFHKLPVEsVHILEDKENVV |
| O43707 | T445 | Sugiyama | ACTN4 | HEAWtDGKEAMLKHRDyEtAtLsDIKALIRKHEAFEsDLAA |
| O43765 | S77 | Sugiyama | SGTA SGT SGT1 | TLPEIFEAAATGKEMPQDLRsPARtPPsEEDsAEAERLKTE |
| O43815 | S373 | Sugiyama | STRN | KLQDMLANLRDVDELPsLQPsVGsPsRPsssRLPEHEINRA |
| O43815 | S378 | Sugiyama | STRN | LANLRDVDELPsLQPsVGsPsRPsssRLPEHEINRADEVEA |
| O43852 | T65 | Sugiyama | CALU | FDyDHDAFLGAEEAKtFDQLtPEEsKERLGKIVSKIDGDKD |
| O60285 | S445 | EPSD|PSP | NUAK1 ARK5 KIAA0537 OMPHK1 | LPSTFKMEQDLCRTGVLLPssPEAEVPGKLsPKQSATMPKK |
| O60292 | S158 | Sugiyama | SIPA1L3 KIAA0545 SPAL3 | FHRLSRRRsKDVEFQDGWPRsPGRAFLPLRHRsssEItLSE |
| O60331 | S650 | GPS6|EPSD|PSP | PIP5K1C KIAA0589 | EEDAPATDIyFPTDERSWVysPLHYSAQAPPAsDGEsDT__ |
| O60346 | S317 | PSP | PHLPP1 KIAA0606 PHLPP PLEKHE1 SCOP | APPADLPLPVGGPGGWsRRAsPAPsDssPGEPFVGGPVssP |
| O60346 | S321 | PSP | PHLPP1 KIAA0606 PHLPP PLEKHE1 SCOP | DLPLPVGGPGGWsRRAsPAPsDssPGEPFVGGPVssPRAPR |
| O60346 | S323 | PSP | PHLPP1 KIAA0606 PHLPP PLEKHE1 SCOP | PLPVGGPGGWsRRAsPAPsDssPGEPFVGGPVssPRAPRPV |
| O60346 | S324 | PSP | PHLPP1 KIAA0606 PHLPP PLEKHE1 SCOP | LPVGGPGGWsRRAsPAPsDssPGEPFVGGPVssPRAPRPVV |
| O60346 | S335 | PSP | PHLPP1 KIAA0606 PHLPP PLEKHE1 SCOP | RAsPAPsDssPGEPFVGGPVssPRAPRPVVsDTESFSLSPS |
| O60346 | S336 | PSP | PHLPP1 KIAA0606 PHLPP PLEKHE1 SCOP | AsPAPsDssPGEPFVGGPVssPRAPRPVVsDTESFSLSPSA |
| O60346 | S345 | PSP | PHLPP1 KIAA0606 PHLPP PLEKHE1 SCOP | PGEPFVGGPVssPRAPRPVVsDTESFSLSPSAESVSDRLDP |
| O60346 | S411 | PSP | PHLPP1 KIAA0606 PHLPP PLEKHE1 SCOP | PGQPRRPGHPAQPLPLPQtAssPQPQQKAPRAIDsPGGAVR |
| O60346 | S412 | PSP | PHLPP1 KIAA0606 PHLPP PLEKHE1 SCOP | GQPRRPGHPAQPLPLPQtAssPQPQQKAPRAIDsPGGAVRE |
| O60346 | S425 | PSP | PHLPP1 KIAA0606 PHLPP PLEKHE1 SCOP | PLPQtAssPQPQQKAPRAIDsPGGAVREGSCEEKAAAAVAP |
| O60346 | S450 | PSP | PHLPP1 KIAA0606 PHLPP PLEKHE1 SCOP | VREGSCEEKAAAAVAPGGLQstPGRSGVTAEKAPPPPPPPT |
| O60346 | T409 | PSP | PHLPP1 KIAA0606 PHLPP PLEKHE1 SCOP | GVPGQPRRPGHPAQPLPLPQtAssPQPQQKAPRAIDsPGGA |
| O60346 | T451 | PSP | PHLPP1 KIAA0606 PHLPP PLEKHE1 SCOP | REGSCEEKAAAAVAPGGLQstPGRSGVTAEKAPPPPPPPTL |
| O60566 | S1043 | EPSD|PSP | BUB1B BUBR1 MAD3L SSK1 | FDTTFQSHLNKALWKVGKLtsPGALLFQ_____________ |
| O60566 | S543 | EPSD|PSP | BUB1B BUBR1 MAD3L SSK1 | GPsVPFSIFDEFLLSEKKNKsPPADPPRVLAQRRPLAVLKt |
| O60566 | S670 | EPSD|PSP | BUB1B BUBR1 MAD3L SSK1 | EDQQTACGtIysQtLsIKKLsPIIEDsREAtHSsGFsGSSA |
| O60566 | T620 | SIGNOR | BUB1B BUBR1 MAD3L SSK1 | tICPNPEDtCDFARAARFVStPFHEIMSLKDLPSDPERLLP |
| O60610 | T768 | EPSD|PSP | DIAPH1 DIAP1 | PPPPPFGFGVPAAPVLPFGLtPKKLYKPEVQLRRPNWSKLV |
| O60701 | T461 | EPSD|PSP | UGDH | GRRVLDGLHNELQTIGFQIEtIGKKVSSKRIPyAPsGEIPK |
| O60841 | S182 | Sugiyama | EIF5B IF2 KIAA0741 | DGsEEDEDNsKKIKERsRINssGEsGDEsDEFLQsRKGQKK |
| O75122 | S1012 | PSP | CLASP2 KIAA0627 | DssQTALDNKAsLLHsMPtHssPRsRDyNPyNysDsIsPFN |
| O75122 | S1013 | PSP|Sugiyama | CLASP2 KIAA0627 | ssQTALDNKAsLLHsMPtHssPRsRDyNPyNysDsIsPFNK |
| O75122 | S1029 | PSP | CLASP2 KIAA0627 | PtHssPRsRDyNPyNysDsIsPFNKsALKEAMFDDDADQFP |
| O75122 | S507 | EPSD|PSP | CLASP2 KIAA0627 | sAsAQKRSKIPRsQGCsREAsPSRLSVARSSRIPRPsVsQG |
| O75122 | S541 | EPSD|PSP | CLASP2 KIAA0627 | RPsVsQGCsREAsRESsRDTsPVRSFQPLASRHHSRSTGAL |
| O75143 | S224 | PSP | ATG13 KIAA0652 | TPPIMGIIIDHFVDRPYPSSsPMHPCNYRTAGEDTGVIYPS |
| O75143 | S44 | PSP | ATG13 KIAA0652 | TVQVIVQARLGEKICTRSSSsPTGSDWFNLAIKDIPEVTHE |
| O75143 | T332 | PSP | ATG13 KIAA0652 | LAPNQPVHGTQADQERLATCtPSDRTHCAAtPSSSEDTEtV |
| O75143 | T342 | PSP | ATG13 KIAA0652 | QADQERLATCtPSDRTHCAAtPSSSEDTEtVsNssEGRAsP |
| O75152 | T321 | EPSD|PSP | ZC3H11A KIAA0663 ZC3HDC11A | RSLAQRLGKKVEAPETNIDKtPKKAQVSKSLKERLGMsADP |
| O75154 | S102 | SIGNOR|EPSD|PSP | RAB11FIP3 ARFO1 KIAA0665 | PRDPGPSAPPPRSGPRGQLAsPDAPGPGPRSEAPLPELDPL |
| O75170 | S771 | SIGNOR|PSP | PPP6R2 KIAA0685 PP6R2 SAPS2 | WAKFTDFQPFCCSESGPRCssPVDTECSHAEGSRSQGPEKA |
| O75306 | S364 | SIGNOR|PSP | NDUFS2 | IAQCLNKMPPGEIKVDDAKVsPPKRAEMKTSMESLIHHFKL |
| O75369 | S1505 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | PSQEGPYMVSVKYADEEIPRsPFKVKVLPTYDASKVtAsGP |
| O75381 | S232 | PSP | PEX14 | LKSEINSLKGLLLNRRQFPPsPSAPKIPSWQIPVKsPsPss |
| O75533 | T207 | Sugiyama | SF3B1 SAP155 | AAAsQPPsKRKRRWDQtADQtPGAtPKKLssWDQAEtPGHt |
| O75533 | T211 | Sugiyama | SF3B1 SAP155 | QPPsKRKRRWDQtADQtPGAtPKKLssWDQAEtPGHtPsLR |
| O75533 | T328 | Sugiyama | SF3B1 SAP155 | sGWAEtPRtDRGGDsIGEtPtPGAsKRKsRWDEtPAsQMGG |
| O75553 | S524 | ELM | DAB1 | PVTSTTPSTNSPPTPAPRQSsPSKSSASHASDPTTDDIFEE |
| O75553 | S548 | ELM | DAB1 | SSASHASDPTTDDIFEEGFEsPSKSEEQEAPDGSQASSNSD |
| O75828 | S56 | Sugiyama | CBR3 SDR21C2 | TARDVARGQAAVQQLQAEGLsPRFHQLDIDDLQsIRALRDF |
| O94761 | S251 | SIGNOR|EPSD|PSP | RECQL4 RECQ4 | GAGSQGPEASAFQEVSIRVGsPQPSSSGGEKRRWNEEPWES |
| O94761 | S89 | EPSD | RECQL4 RECQ4 | AEEAPEPRCWGPHLNRAAtKsPQStPGRSRQGsVPDYGQRL |
| O94762 | S727 | EPSD|PSP | RECQL5 RECQ5 | EPLPGPRGEVPGGSAHyGGPsPEKKAKSSSGGSSLAKGRAS |
| O94776 | S435 | Sugiyama | MTA2 MTA1L1 PID | RGtTEPHSRGHLsRPEAQsLsPyttsANRAKLLAKNRQtFL |
| O94782 | S313 | SIGNOR|EPSD|PSP | USP1 | LEENQRQTRSKRKATSDTLEsPPKIIPKYIsENEsPRPsQK |
| O94901 | S48 | SIGNOR|PSP | SUN1 KIAA0810 UNC84A | SYSSDALDFETEHKLDPVFDsPRMSRRsLRLATTACTLGDG |
| O94916 | T135 | SIGNOR | NFAT5 KIAA0827 TONEBP | SNRGVsEKQLTSNTVQQHPstPKRHTVLyIsPPPEDLLDNs |
| O94979 | S799 | Sugiyama | SEC31A KIAA0905 SEC31L1 HSPC275 HSPC334 | IMQLRDRLCRAQGEPVAGHEsPKIPyEKQQLPKGRPGPVAG |
| O95139 | S29 | SIGNOR|PSP | NDUFB6 | KLRLQQLRELRRRWLKDQELsPREPVLPPQKMGPMEKFWNK |
| O95139 | S55 | SIGNOR|PSP | NDUFB6 | LPPQKMGPMEKFWNKFLENKsPWRKMVHGVYKKSIFVFTHV |
| O95139 | T5 | SIGNOR|PSP | NDUFB6 | ________________MTGYtPDEKLRLQQLRELRRRWLKD |
| O95235 | S21 | PSP | KIF20A MKLP2 RAB6KIFL | MsQGILsPPAGLLsDDDVVVsPMFESTAADLGsVVRKNLLs |
| O95235 | S532 | PSP | KIF20A MKLP2 RAB6KIFL | PMQLGFPSLHSFIKEHsLQVsPsLEKGAKADTGLDDDIENE |
| O95235 | S7 | PSP | KIF20A MKLP2 RAB6KIFL | ______________MsQGILsPPAGLLsDDDVVVsPMFEST |
| O95235 | S867 | PSP | KIF20A MKLP2 RAB6KIFL | KPFLRNLLPRtPtCQSStDCsPyARILRSRRsPLLKsGPFG |
| O95235 | S878 | PSP | KIF20A MKLP2 RAB6KIFL | PtCQSStDCsPyARILRSRRsPLLKsGPFGKKY________ |
| O95235 | T198 | PSP | KIF20A MKLP2 RAB6KIFL | GILPRSLALIFNSLQGQLHPtPDLKPLLSNEVIWLDSKQIR |
| O95235 | T857 | PSP | KIF20A MKLP2 RAB6KIFL | QQPNQQPPGKKPFLRNLLPRtPtCQSStDCsPyARILRSRR |
| O95239 | T1161 | SIGNOR|EPSD|PSP | KIF4A KIF4 | KLEDPTEVTPGLSFFNPVCAtPNSKILKEMCDVEQVLSKKt |
| O95251 | T85 | SIGNOR|EPSD|PSP | KAT7 HBO1 HBOa MYST2 | FGTEEPAYstRRVTRsQQQPtPVtPKKYPLRQtRssGsEtE |
| O95251 | T88 | SIGNOR|EPSD|PSP | KAT7 HBO1 HBOa MYST2 | EEPAYstRRVTRsQQQPtPVtPKKYPLRQtRssGsEtEQVV |
| O95297 | S210 | Sugiyama | MPZL1 PZR UNQ849/PRO1787 | LYRRKNSKRDyTGCstsEsLsPVKQAPRKsPsDtEGLVKSL |
| O95359 | S2317 | Sugiyama | TACC2 | MPLRRPKMKKtPEKLDNtPAsPPRsPAEPNDIPIAKGTYTF |
| O95359 | S2321 | Sugiyama | TACC2 | RPKMKKtPEKLDNtPAsPPRsPAEPNDIPIAKGTYTFDIDK |
| O95394 | S64 | Sugiyama | PGM3 AGM1 | LLAVLRSKQTKSTIGVMVtAsHNPEEDNGVKLVDPLGEMLA |
| O95425 | S920 | Sugiyama | SVIL | LDHNAsAtDYKFSssIENsDsPVRSILKSQAWQPLVEGsEN |
| O95747 | S359 | Sugiyama | OXSR1 KIAA1101 OSR1 | sDDEFDEEsEEGKAAIsQLRsPRVKESISNSELFPTTDPVG |
| O95817 | S284 | PSP | BAG3 BIS | sPFRssVQGAssREGsPARsstPLHsPsPIRVHtVVDRPQQ |
| O95817 | S289 | PSP|Sugiyama | BAG3 BIS | sVQGAssREGsPARsstPLHsPsPIRVHtVVDRPQQPMTHR |
| O95817 | S291 | PSP | BAG3 BIS | QGAssREGsPARsstPLHsPsPIRVHtVVDRPQQPMTHRET |
| O95817 | T285 | PSP | BAG3 BIS | PFRssVQGAssREGsPARsstPLHsPsPIRVHtVVDRPQQP |
| O95835 | S613 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | LATS1 WARTS | sEKSYENVDSGDKEKKQIttsPItVRKNKKDEERRESRIQS |
| O95835 | T490 | iPTMNet|EPSD|PSP | LATS1 WARTS | GNRASHSANSQPSATTVTAItPAPIQQPVKSMRVLKPELQT |
| O95997 | S165 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | PTTG1 EAP1 PTTG TUTR1 | PLMILDEERELEKLFQLGPPsPVKMPsPPWESNLLQsPssI |
| O96019 | S233 | Sugiyama | ACTL6A BAF53 BAF53A INO80K | MNIELVPPYMIASKEAVREGsPANWKRKEKLPQVTRSWHNY |
| P00338 | S161 | Sugiyama | LDHA PIG19 | DILTYVAWKISGFPKNRVIGsGCNLDsARFRyLMGERLGVH |
| P00338 | T248 | EPSD|PSP | LDHA PIG19 | KEVHKQVVEsAyEVIKLKGYtSWAIGLSVADLAESIMKNLR |
| P00533 | S1026 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | EGFR ERBB ERBB1 HER1 | DMDDVVDADEyLIPQQGFFssPStsRTPLLssLsAtsNNst |
| P00558 | T168 | Sugiyama | PGK1 PGKA MIG10 OK/SW-cl.110 | EAFRAsLSKLGDVyVNDAFGtAHRAHssMVGVNLPQKAGGF |
| P02545 | S22 | SIGNOR|ELM|iPTMNet|EPSD|PSP | LMNA LMN1 | ETPsQRRAtRsGAQAsstPLsPtRItRLQEKEDLQELNDRL |
| P02545 | S390 | SIGNOR|EPSD|PSP | LMNA LMN1 | DMEIHAYRKLLEGEEERLRLsPsPtsQRsRGRAssHssQtQ |
| P02545 | S392 | SIGNOR|iPTMNet|EPSD|PSP | LMNA LMN1 | EIHAYRKLLEGEEERLRLsPsPtsQRsRGRAssHssQtQGG |
| P02545 | T19 | ELM|iPTMNet|EPSD|PSP | LMNA LMN1 | __METPsQRRAtRsGAQAsstPLsPtRItRLQEKEDLQELN |
| P03372 | S104 | ELM | ESR1 ESR NR3A1 | SEAAAFGSNGLGGFPPLNsVsPsPLMLLHPPPQLsPFLQPH |
| P03372 | S106 | ELM | ESR1 ESR NR3A1 | AAAFGSNGLGGFPPLNsVsPsPLMLLHPPPQLsPFLQPHGQ |
| P03973 | T78 | Sugiyama | SLPI WAP4 WFDC4 | PGKKRCCPDTCGIKCLDPVDtPNPTRRKPGKCPVTYGQCLM |
| P04075 | S309 | Sugiyama | ALDOA ALDA | KCPLLKPWALTFSYGRALQAsALKAWGGKKENLKAAQEEYV |
| P04075 | S36 | Sugiyama | ALDOA ALDA | LsDIAHRIVAPGKGILAADEstGsIAKRLQsIGtENtEENR |
| P04075 | S39 | Sugiyama | ALDOA ALDA | IAHRIVAPGKGILAADEstGsIAKRLQsIGtENtEENRRFy |
| P04075 | T37 | Sugiyama | ALDOA ALDA | sDIAHRIVAPGKGILAADEstGsIAKRLQsIGtENtEENRR |
| P04179 | S106 | EPSD|PSP | SOD2 | PALKFNGGGHINHSIFWTNLsPNGGGEPKGELLEAIKRDFG |
| P04183 | S13 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | TK1 | ________MSCINLPTVLPGsPsKtRGQIQVILGPMFSGKS |
| P04406 | S210 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | GPsGKLWRDGRGALQNIIPAstGAAKAVGKVIPELNGKLtG |
| P04406 | T211 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | PsGKLWRDGRGALQNIIPAstGAAKAVGKVIPELNGKLtGM |
| P04637 | S315 | GPS6|SIGNOR|EPSD|PSP | TP53 P53 | PHHELPPGStKRALPNNTsssPQPKKKPLDGEyFTLQIRGR |
| P04637 | S33 | ELM | TP53 P53 | PLsQEtFsDLWKLLPENNVLsPLPsQAMDDLMLsPDDIEQW |
| P04792 | S82 | Sugiyama | HSPB1 HSP27 HSP28 | AIEsPAVAAPAYsRALsRQLssGVsEIRHtADRWRVsLDVN |
| P05023 | S722 | Sugiyama | ATP1A1 | VEGCQRQGAIVAVTGDGVNDsPALKKADIGVAMGIAGSDVS |
| P05067 | T743 | EPSD|PSP | APP A4 AD1 | LKKKQYtsIHHGVVEVDAAVtPEERHLSKMQQNGyENPtyK |
| P05187 | S177 | Sugiyama | ALPP PLAP | RAKKAGKSVGVVTTTRVQHAsPAGtyAHtVNRNWysDADVP |
| P05187 | S436 | Sugiyama | ALPP PLAP | GNGPGYVLKDGARPDVtEsEsGsPEyRQQSAVPLDEETHAG |
| P05187 | S438 | Sugiyama | ALPP PLAP | GPGYVLKDGARPDVtEsEsGsPEyRQQSAVPLDEETHAGED |
| P05783 | S34 | GPS6|SIGNOR|iPTMNet|EPSD | KRT18 CYK18 PIG46 | RsLGsVQAPsyGARPVssAAsVyAGAGGsGsRIsVsRstsF |
| P05787 | S432 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | KRT8 CYK8 | HtKTTSGYAGGLSSAYGGLtsPGLSYSLGSSFGSGAGSSSF |
| P06400 | S249 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RB1 | LsPPMLLKEPYKTAVIPINGsPRtPRRGQNRSARIAKQLEN |
| P06400 | S807 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RB1 | RsPyKFPssPLRIPGGNIyIsPLKsPYKIsEGLPtPtKMtP |
| P06400 | S811 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RB1 | KFPssPLRIPGGNIyIsPLKsPYKIsEGLPtPtKMtPRSRI |
| P06400 | T252 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RB1 | PMLLKEPYKTAVIPINGsPRtPRRGQNRSARIAKQLENDTR |
| P06400 | T373 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RB1 | tQRtPRKsNLDEEVNVIPPHtPVRTVMNTIQQLMMILNSAS |
| P06493 | S178 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | RVytHEVVTLWYRSPEVLLGsARYSTPVDIWSIGTIFAELA |
| P06493 | S46 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | TGQVVAMKKIRLEsEEEGVPstAIREIsLLKELRHPNIVSL |
| P06493 | T14 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | _______MEDyTKIEKIGEGtyGVVyKGRHKTTGQVVAMKK |
| P06493 | T47 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | GQVVAMKKIRLEsEEEGVPstAIREIsLLKELRHPNIVSLQ |
| P06493 | Y15 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | ______MEDyTKIEKIGEGtyGVVyKGRHKTTGQVVAMKKI |
| P06493 | Y19 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | __MEDyTKIEKIGEGtyGVVyKGRHKTTGQVVAMKKIRLEs |
| P06733 | S263 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | GMDVAASEFFRsGKyDLDFKsPDDPsRyIsPDQLADLyKsF |
| P06733 | S272 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | FRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyPVVsI |
| P06733 | T100 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | KKLNVtEQEKIDKLMIEMDGtENKsKFGANAILGVsLAVCK |
| P06733 | T205 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | GAEVyHNLKNVIKEKyGKDAtNVGDEGGFAPNILENKEGLE |
| P06744 | S455 | Sugiyama | GPI | ALMRGKSTEEARKELQAAGKsPEDLERLLPHKVFEGNRPTN |
| P06748 | S70 | SIGNOR|EPSD|PSP | NPM1 NPM | GAGAKDELHIVEAEAMNyEGsPIKVtLAtLKMsVQPtVsLG |
| P06748 | T199 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | NPM1 NPM | DDFDDEEAEEKAPVKKsIRDtPAKNAQKSNQNGKDsKPsst |
| P06748 | T219 | GPS6|iPTMNet|EPSD|PSP | NPM1 NPM | tPAKNAQKSNQNGKDsKPsstPRsKGQEsFKKQEKtPKtPK |
| P06748 | T234 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | NPM1 NPM | sKPsstPRsKGQEsFKKQEKtPKtPKGPssVEDIKAKMQAs |
| P06748 | T237 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | NPM1 NPM | sstPRsKGQEsFKKQEKtPKtPKGPssVEDIKAKMQAsIEK |
| P07195 | S162 | Sugiyama | LDHB | DILTYVTWKLSGLPKHRVIGsGCNLDsARFRyLMAEKLGIH |
| P07195 | S303 | Sugiyama | LDHB | GIENEVFLSLPCILNARGLtsVINQKLKDDEVAQLKKsADt |
| P07195 | T302 | Sugiyama | LDHB | YGIENEVFLSLPCILNARGLtsVINQKLKDDEVAQLKKsAD |
| P07195 | T323 | Sugiyama | LDHB | sVINQKLKDDEVAQLKKsADtLWDIQKDLKDL_________ |
| P07205 | T168 | Sugiyama | PGK2 PGKB | EAFRAsLSKLGDVyVNDAFGtAHRAHSSMVGVNLPHKASGF |
| P07437 | S115 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | sGAGNNWAKGHytEGAELVDsVLDVVRKEAESCDCLQGFQL |
| P07437 | S75 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | tGGKyVPRAILVDLEPGtMDsVRsGPFGQIFRPDNFVFGQs |
| P07437 | T55 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | tyHGDsDLQLDRIsVyyNEAtGGKyVPRAILVDLEPGtMDs |
| P07814 | S886 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | EKTGKEyIPGQPPLsQssDssPtRNsEPAGLEtPEAKVLFD |
| P07858 | S216 | Sugiyama | CTSB CPSB | PPCTGEGDTPKCSKICEPGysPtyKQDKHYGYNSYSVSNSE |
| P07864 | S161 | Sugiyama | LDHC LDH3 LDHX | DILTYIVWKISGLPVTRVIGsGCNLDsARFRYLIGEKLGVH |
| P07900 | S391 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | MDNCEELIPEYLNFIRGVVDsEDLPLNIsREMLQQsKILKV |
| P07900 | S505 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | KENQKHIyyItGETKDQVANsAFVERLRKHGLEVIyMIEPI |
| P07900 | T109 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | LtIVDtGIGMTKADLINNLGtIAKSGtKAFMEALQAGADIS |
| P07900 | T65 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | LRELIsNssDALDKIRyEsLtDPsKLDsGKELHINLIPNKQ |
| P08047 | S720 | PSP | SP1 TSFP1 | HLsKHIKTHQNKKGGPGVALsVGtLPLDsGAGsEGSGtAtP |
| P08047 | T723 | PSP | SP1 TSFP1 | KHIKTHQNKKGGPGVALsVGtLPLDsGAGsEGSGtAtPSAL |
| P08047 | T737 | PSP | SP1 TSFP1 | VALsVGtLPLDsGAGsEGSGtAtPSALITTNMVAMEAICPE |
| P08047 | T739 | SIGNOR|EPSD|PSP | SP1 TSFP1 | LsVGtLPLDsGAGsEGSGtAtPSALITTNMVAMEAICPEGI |
| P08195 | S296 | Sugiyama | SLC3A2 MDU1 | DLLQIDPNFGsKEDFDsLLQsAKKKSIRVILDLTPNYRGEN |
| P08195 | S598 | Sugiyama | SLC3A2 MDU1 | LQASDLPASASLPAKADLLLstQPGREEGsPLELERLKLEP |
| P08195 | S607 | Sugiyama | SLC3A2 MDU1 | ASLPAKADLLLstQPGREEGsPLELERLKLEPHEGLLLRFP |
| P08238 | S383 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | MDSCDELIPEYLNFIRGVVDsEDLPLNIsREMLQQsKILKV |
| P08238 | S497 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | KEtQKsIyyItGEsKEQVANsAFVERVRKRGFEVVyMtEPI |
| P08238 | S535 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | EPIDEyCVQQLKEFDGKsLVsVtKEGLELPEDEEEKKKMEE |
| P08238 | T104 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | LtLVDtGIGMtKADLINNLGtIAKSGtKAFMEALQAGADIS |
| P08238 | T60 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | LRELIsNAsDALDKIRyEsLtDPsKLDsGKELKIDIIPNPQ |
| P08651 | S323 | Sugiyama | NFIC NFI | PssPtsSSRNWTEDMEGGIssPVKKtEMDKsPFNsPsPQDs |
| P08670 | S55 | SIGNOR|EPSD|PSP | VIM | TRtYsLGsALRPstsRsLyAssPGGVyAtRssAVRLRssVP |
| P08670 | S56 | GPS6|ELM|iPTMNet|EPSD|PSP | VIM | RtYsLGsALRPstsRsLyAssPGGVyAtRssAVRLRssVPG |
| P08865 | T97 | Sugiyama | RPSA LAMBR LAMR1 | IssRNtGQRAVLKFAAAtGAtPIAGRFtPGTFTNQIQAAFR |
| P09234 | S17 | Sugiyama | SNRPC | ____MPKFyCDyCDtyLtHDsPsVRKTHCSGRKHKENVKDY |
| P09651 | S6 | Sugiyama | HNRNPA1 HNRPA1 | _______________MsKsEsPKEPEQLRKLFIGGLsFEtT |
| P09923 | S174 | Sugiyama | ALPI | RAKQAGKSVGVVTTTRVQHAsPAGtyAHtVNRNWysDADMP |
| P0C1Z6 | S180 | EPSD|PSP | TFPT INO80F | PPEKEtLsPPRRtPAPPEPGsPAPGEGPsGRKRRRVPRDGR |
| P0DPH7 | T56 | Sugiyama | TUBA3C TUBA2 | MPSDKtIGGGDDsFNtFFsEtGAGKHVPRAVFVDLEPtVVD |
| P10275 | S310 | EPSD|PSP | AR DHTR NR3C4 | CKGsLLDDSAGKstEDTAEYsPFKGGYTKGLEGESLGCSGS |
| P10275 | S516 | EPSD|PSP | AR DHTR NR3C4 | DFTAPDVWYPGGMVSRVPYPsPTCVKSEMGPWMDSYSGPyG |
| P10275 | S83 | SIGNOR|EPSD|PSP | AR DHTR NR3C4 | QQQQQQQQQQQQQQQQQQETsPRQQQQQQGEDGsPQAHRRG |
| P10412 | T18 | EPSD|PSP|Sugiyama | H1-4 H1F4 HIST1H1E | ___MsEtAPAAPAAPAPAEKtPVKKKARKsAGAAKRKAsGP |
| P10415 | S87 | PSP | BCL2 | ARtsPLQtPAAPGAAAGPALsPVPPVVHLTLRQAGDDFSRR |
| P10415 | T56 | SIGNOR|EPSD|PSP | BCL2 | GAAPPGAAPAPGIFSSQPGHtPHPAASRDPVARtsPLQtPA |
| P10415 | T69 | PSP | BCL2 | FSSQPGHtPHPAASRDPVARtsPLQtPAAPGAAAGPALsPV |
| P10636 | S519 | ELM | MAPT MAPTL MTBT1 TAU | PPsSGEPPKsGDRsGyssPGsPGtPGsRsRtPsLPtPPTRE |
| P10636 | S552 | ELM | MAPT MAPTL MTBT1 TAU | LPtPPTREPKKVAVVRtPPKsPssAKSRLQTAPVPMPDLKN |
| P10636 | S713 | ELM | MAPT MAPTL MTBT1 TAU | LTFRENAKAKTDHGAEIVyKsPVVsGDtsPRHLsNVsstGs |
| P10636 | S721 | ELM | MAPT MAPTL MTBT1 TAU | AKTDHGAEIVyKsPVVsGDtsPRHLsNVsstGsIDMVDsPQ |
| P10636 | T522 | ELM | MAPT MAPTL MTBT1 TAU | SGEPPKsGDRsGyssPGsPGtPGsRsRtPsLPtPPTREPKK |
| P10636 | T529 | ELM | MAPT MAPTL MTBT1 TAU | GDRsGyssPGsPGtPGsRsRtPsLPtPPTREPKKVAVVRtP |
| P10636 | T534 | ELM | MAPT MAPTL MTBT1 TAU | yssPGsPGtPGsRsRtPsLPtPPTREPKKVAVVRtPPKsPs |
| P10636 | T548 | ELM | MAPT MAPTL MTBT1 TAU | RtPsLPtPPTREPKKVAVVRtPPKsPssAKSRLQTAPVPMP |
| P10636 | T690 | ELM | MAPT MAPTL MTBT1 TAU | KIGsLDNITHVPGGGNKKIEtHKLTFRENAKAKTDHGAEIV |
| P10636 | T95 | iPTMNet | MAPT MAPTL MTBT1 TAU | VTAPLVDEGAPGKQAAAQPHtEIPEGTTAEEAGIGDtPSLE |
| P10696 | S433 | Sugiyama | ALPG ALPPL ALPPL2 | GNGPGYVLKDGARPDVtEsEsGsPEyRQQSAVPLDGETHAG |
| P10696 | S435 | Sugiyama | ALPG ALPPL ALPPL2 | GPGYVLKDGARPDVtEsEsGsPEyRQQSAVPLDGETHAGED |
| P10809 | S225 | Sugiyama | HSPD1 HSP60 | KtLNDELEIIEGMKFDRGyIsPyFINtsKGQKCEFQDAyVL |
| P10809 | S70 | Sugiyama | HSPD1 HSP60 | AVAVTMGPKGRtVIIEQsWGsPKVTKDGVtVAKsIDLKDKY |
| P11142 | S85 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | NtVFDAKRLIGRRFDDAVVQsDMKHWPFMVVNDAGRPKVQV |
| P11142 | T64 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | FtDtERLIGDAAKNQVAMNPtNtVFDAKRLIGRRFDDAVVQ |
| P11142 | T66 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | DtERLIGDAAKNQVAMNPtNtVFDAKRLIGRRFDDAVVQsD |
| P11171 | S712 | GPS6|EPSD | EPB41 E41P | FMESVPEPRPSEWDKRLstHsPFRTLNINGQIPTGEGPPLV |
| P11171 | T60 | GPS6|EPSD|PSP | EPB41 E41P | QTAAEGDNWCEQKLKASNGDtPTHEDLTKNKERTSESRGLS |
| P11387 | S112 | SIGNOR|EPSD|PSP | TOP1 | EKVRASGDAKIKKEKENGFssPPQIKDEPEDDGYFVPPKED |
| P11387 | S394 | SIGNOR|EPSD|PSP | TOP1 | KRRIMPEDIIINCSKDAKVPsPPPGHKWKEVRHDNKVTWLV |
| P11388 | S1213 | GPS6|ELM|iPTMNet|EPSD|PSP | TOP2A TOP2 | LPGKGGKAKGKKTQMAEVLPsPRGQRVIPRITIEMKAEAEK |
| P11388 | S1247 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | TOP2A TOP2 | MKAEAEKKNKKKIKNENtEGsPQEDGVELEGLKQRLEKKQK |
| P11388 | S1354 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | TOP2A TOP2 | EDFsDFDEKtDDEDFVPsDAsPPKtKTsPKLsNKELKPQKs |
| P11388 | S1361 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | TOP2A TOP2 | EKtDDEDFVPsDAsPPKtKTsPKLsNKELKPQKsVVsDLEA |
| P11388 | S1393 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | TOP2A TOP2 | KsVVsDLEADDVKGsVPLsssPPAtHFPDEtEItNPVPKKN |
| P12270 | S2073 | EPSD|PSP | TPR | VsREQQPSsASERQAPRAPQsPRRPPHPLPPRLTIHAPPQE |
| P12270 | S2155 | Sugiyama | TPR | PstPtLVVPHRtDGFAEAIHsPQVAGVPRFRFGPPEDMPQT |
| P12272 | T108 | GPS6|ELM|iPTMNet|EPSD | PTHLH PTHRP | TKNHPVRFGSDDEGRYLTQEtNKVETYKEQPLKtPGKKKKG |
| P12272 | T121 | SIGNOR | PTHLH PTHRP | GRYLTQEtNKVETYKEQPLKtPGKKKKGKPGKRKEQEKKKR |
| P12931 | S75 | ELM | SRC SRC1 | APAAAEPKLFGGFNssDtVtsPQRAGPLAGGVTTFVALyDY |
| P13051 | S12 | SIGNOR | UNG DGU UNG1 UNG15 | _________MIGQKtLysFFsPsPARKRHAPsPEPAVQGtG |
| P13051 | S14 | SIGNOR | UNG DGU UNG1 UNG15 | _______MIGQKtLysFFsPsPARKRHAPsPEPAVQGtGVA |
| P13051 | S23 | SIGNOR | UNG DGU UNG1 UNG15 | GQKtLysFFsPsPARKRHAPsPEPAVQGtGVAGVPEESGDA |
| P13051 | S64 | SIGNOR|EPSD|PSP | UNG DGU UNG1 UNG15 | AAIPAKKAPAGQEEPGtPPssPLsAEQLDRIQRNKAAALLR |
| P13051 | T60 | SIGNOR | UNG DGU UNG1 UNG15 | SGDAAAIPAKKAPAGQEEPGtPPssPLsAEQLDRIQRNKAA |
| P13637 | S712 | Sugiyama | ATP1A3 | VEGCQRQGAIVAVTGDGVNDsPALKKADIGVAMGIAGSDVS |
| P13639 | S593 | Sugiyama | EEF2 EF2 | SDPVVsyREtVsEEsNVLCLsKsPNKHNRLyMKARPFPDGL |
| P13639 | S595 | PSP|Sugiyama | EEF2 EF2 | PVVsyREtVsEEsNVLCLsKsPNKHNRLyMKARPFPDGLAE |
| P13804 | S192 | Sugiyama | ETFA | sFDAAATsGGsASsEKAsStsPVEIsEWLDQKLTKSDRPEL |
| P14136 | S8 | iPTMNet | GFAP | _____________MERRRItsAARRsYVssGEMMVGGLAPG |
| P14314 | S442 | Sugiyama | PRKCSH G19P1 | EYVYRLCPFKLVSQKPKLGGsPtsLGtWGsWIGPDHDKFSA |
| P14618 | S202 | Sugiyama | PKM OIP3 PK2 PK3 PKM2 | SLQVKQKGADFLVtEVENGGsLGsKKGVNLPGAAVDLPAVs |
| P14618 | S37 | PSP|Sugiyama | PKM OIP3 PK2 PK3 PKM2 | QLHAAMADTFLEHMCRLDIDsPPItARNtGIICtIGPAsRs |
| P14618 | T41 | Sugiyama | PKM OIP3 PK2 PK3 PKM2 | AMADTFLEHMCRLDIDsPPItARNtGIICtIGPAsRsVEtL |
| P14625 | S552 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | KEKQDKIyFMAGsSRKEAEssPFVERLLKKGyEVIyLTEPV |
| P14625 | S680 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | RIMKAQAYQtGKDIstNyyAsQKKTFEINPRHPLIRDMLRR |
| P14635 | S126 | GPS6|EPSD|PSP | CCNB1 CCNB | EPEPVKEEKLsPEPILVDTAsPsPMETsGCAPAEEDLCQAF |
| P14635 | S128 | EPSD|PSP | CCNB1 CCNB | EPVKEEKLsPEPILVDTAsPsPMETsGCAPAEEDLCQAFsD |
| P14866 | S101 | Sugiyama | HNRNPL HNRPL P/OKcl.14 | GAAGGGGGGENyDDPHKtPAsPVVHIRGLIDGVVEADLVEA |
| P15172 | S200 | SIGNOR|ELM|iPTMNet|EPSD | MYOD1 BHLHC1 MYF3 MYOD | APGPLPPGRGGEHYSGDSDAssPRSNCSDGMMDYSGPPSGA |
| P15172 | S201 | GPS6|EPSD | MYOD1 BHLHC1 MYF3 MYOD | PGPLPPGRGGEHYSGDSDAssPRSNCSDGMMDYSGPPSGAR |
| P15172 | S5 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | MYOD1 BHLHC1 MYF3 MYOD | ________________MELLsPPLRDVDLTAPDGSLCSFAT |
| P15531 | S120 | SIGNOR|EPSD|PSP | NME1 NDPKA NM23 | KPGtIRGDFCIQVGRNIIHGsDsVEsAEKEIGLWFHPEELV |
| P15531 | T94 | EPSD|PSP | NME1 NDPKA NM23 | VAMVWEGLNVVKTGRVMLGEtNPADsKPGtIRGDFCIQVGR |
| P15927 | S23 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RPA2 REPA2 RPA32 RPA34 | NsGFEsYGsssYGGAGGYtQsPGGFGsPAPsQAEKKSRARA |
| P15927 | S29 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RPA2 REPA2 RPA32 RPA34 | YGsssYGGAGGYtQsPGGFGsPAPsQAEKKSRARAQHIVPC |
| P15927 | S33 | EPSD|PSP | RPA2 REPA2 RPA32 RPA34 | sYGGAGGYtQsPGGFGsPAPsQAEKKSRARAQHIVPCTIsQ |
| P16152 | S56 | Sugiyama | CBR1 CBR CRN SDR21C1 | TARDVTRGQAAVQQLQAEGLsPRFHQLDIDDLQsIRALRDF |
| P16220 | S256 | PSP | CREB1 | QTYQIRTAPTSTIAPGVVMAssPALPTQPAEEAARKREVRL |
| P16220 | S257 | PSP | CREB1 | TYQIRTAPTSTIAPGVVMAssPALPTQPAEEAARKREVRLM |
| P16949 | S25 | GPS6|iPTMNet|EPSD|PSP | STMN1 C1orf215 LAP18 OP18 | DIQVKELEKRAsGQAFELILsPRsKEsVPEFPLsPPKKKDL |
| P16949 | S38 | GPS6|ELM|iPTMNet|EPSD|PSP|Sugiyama | STMN1 C1orf215 LAP18 OP18 | QAFELILsPRsKEsVPEFPLsPPKKKDLsLEEIQKKLEAAE |
| P17096 | S36 | GPS6|SIGNOR|EPSD|PSP | HMGA1 HMGIY | QEKDGTEKRGRGRPRKQPPVsPGtALVGsQKEPsEVPtPKR |
| P17096 | T53 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | HMGA1 HMGIY | PPVsPGtALVGsQKEPsEVPtPKRPRGRPKGsKNKGAAKTR |
| P17096 | T78 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | HMGA1 HMGIY | RGRPKGsKNKGAAKTRKTTTtPGRKPRGRPKKLEKEEEEGI |
| P17302 | S255 | PSP | GJA1 GJAL | GVKDRVKGKSDPyHATsGALsPAKDCGsQKyAyFNGCssPt |
| P17302 | S262 | PSP | GJA1 GJAL | GKSDPyHATsGALsPAKDCGsQKyAyFNGCssPtAPLsPMs |
| P17544 | T51 | Sugiyama | ATF7 ATFA | HEMTLKFGPARtDsVIIADQtPtPtRFLKNCEEVGLFNELA |
| P17600 | S551 | ELM | SYN1 | RQSRPVAGGPGAPPAARPPAsPsPQRQAGPPQATRQTsVSG |
| P17706 | S304 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP|Sugiyama | PTPN2 PTPT | SIQKRWKELsKEDLsPAFDHsPNKIMtEKYNGNRIGLEEEK |
| P17812 | S575 | Sugiyama | CTPS1 CTPS | LQKGCRLsPRDtysDRsGsssPDsEItELKFPsINHD____ |
| P17980 | S376 | Sugiyama | PSMC3 TBP1 | MPNEEARARIMQIHSRKMNVsPDVNyEELARCTDDFNGAQC |
| P18031 | S386 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | PTPN1 PTP1B | QDtEVRSRVVGGsLRGAQAAsPAKGEPsLPEKDEDHALSYW |
| P18124 | T17 | Sugiyama | RPL7 | ____MEGVEEKKKEVPAVPEtLKKKRRNFAELKIKRLRKKF |
| P18621 | T79 | Sugiyama | RPL17 | PFRRYNGGVGRCAQAKQWGWtQGRWPKKSAEFLLHMLKNAE |
| P18669 | S31 | Sugiyama | PGAM1 PGAMA CDABP0006 | HGEsAWNLENRFsGWyDADLsPAGHEEAKRGGQALRDAGyE |
| P18754 | S11 | SIGNOR|EPSD|PSP | RCC1 CHC1 | __________MsPKRIAKRRsPPADAIPKsKKVKVsHRsHs |
| P18754 | S2 | SIGNOR|iPTMNet | RCC1 CHC1 | ___________________MsPKRIAKRRsPPADAIPKsKK |
| P18754 | S387 | SIGNOR|EPSD|PSP | RCC1 CHC1 | FAWGMGTNYQLGTGQDEDAWsPVEMMGKQLENRVVLSVSSG |
| P18754 | T274 | SIGNOR|EPSD|PSP | RCC1 CHC1 | AISHEGHVYGFGLSNYHQLGtPGTESCFIPQNLTSFKNSTK |
| P18858 | S51 | Sugiyama | LIG1 | TEPPPKAALKEWNGVVsEsDsPVKRPGRKAARVLGsEGEEE |
| P18858 | S76 | SIGNOR|EPSD|PSP | LIG1 | PGRKAARVLGsEGEEEDEALsPAKGQKPALDCsQVsPPRPA |
| P18887 | S447 | Sugiyama | XRCC1 | KLPQKQPQTKtKPtQAAGPssPQKPPtPEEtKAAsPVLQED |
| P18887 | T453 | Sugiyama | XRCC1 | PQTKtKPtQAAGPssPQKPPtPEEtKAAsPVLQEDIDIEGV |
| P18887 | T457 | Sugiyama | XRCC1 | tKPtQAAGPssPQKPPtPEEtKAAsPVLQEDIDIEGVQsEG |
| P19338 | T121 | EPSD|PSP | NCL | AKAVTtPGKKGAtPGKALVAtPGKKGAAIPAKGAKNGKNAK |
| P19338 | T464 | Sugiyama | NCL | KTFEEKQGtEIDGRsIsLyytGEKGQNQDYRGGKNSTWsGE |
| P19338 | T641 | EPSD|PSP | NCL | EDAKAAKEAMEDGEIDGNKVtLDWAKPKGEGGFGGRGGGRG |
| P19338 | T707 | EPSD|PSP | NCL | RGGFRGGRGGGGDHKPQGKKtKFE_________________ |
| P19525 | S456 | PSP | EIF2AK2 PKR PRKR | VtsLKNDGKRtRSKGtLRyMsPEQIssQDYGKEVDLYALGL |
| P19525 | S83 | PSP | EIF2AK2 PKR PRKR | AKNAAAKLAVEILNKEKKAVsPLLLtttNssEGLsMGNyIG |
| P20338 | S204 | iPTMNet|EPSD|PSP | RAB4A RAB4 | DPERMGsGIQYGDAALRQLRsPRRAQAPNAQECGC______ |
| P20700 | S23 | ELM|iPTMNet|EPSD|PSP|Sugiyama | LMNB1 LMN2 LMNB | TAtPVPPRMGsRAGGPttPLsPtRLsRLQEKEELRELNDRL |
| P20700 | S393 | ELM|EPSD|PSP | LMNB1 LMN2 LMNB | EIsAYRKLLEGEEERLKLsPsPssRVtVsRAsssRsVRTTR |
| P21333 | S1084 | EPSD|PSP|Sugiyama | FLNA FLN FLN1 | PTKPSKVKAFGPGLQGGsAGsPARFtIDTKGAGTGGLGLTV |
| P21333 | S1436 | EPSD|PSP | FLNA FLN FLN1 | PyEAGtYSLNVTYGGHQVPGsPFKVPVHDVTDASKVKCsGP |
| P21333 | S1459 | EPSD|PSP | FLNA FLN FLN1 | KVPVHDVTDASKVKCsGPGLsPGMVRANLPQsFQVDTSKAG |
| P21333 | S1533 | EPSD|PSP|Sugiyama | FLNA FLN FLN1 | PSREGPysIsVLyGDEEVPRsPFKVKVLPTHDASKVKAsGP |
| P21333 | S1630 | EPSD|PSP | FLNA FLN FLN1 | PDVTGRYTILIKYGGDEIPFsPyRVRAVPTGDASKCTVTVS |
| P21333 | S2640 | Sugiyama | FLNA FLN FLN1 | LKDKGEYTLVVKWGDEHIPGsPYRVVVP_____________ |
| P22234 | S27 | EPSD|PSP|Sugiyama | PAICS ADE2 AIRC PAIS | LNIGKKLYEGKtKEVyELLDsPGKVLLQsKDQItAGNAARK |
| P22314 | S4 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | UBA1 A1S9T UBE1 | _________________MSSsPLSKKRRVsGPDPKPGsNCs |
| P22314 | S835 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | UBA1 A1S9T UBE1 | QsANAsVDDsRLEELKATLPsPDKLPGFKMyPIDFEKDDDS |
| P22314 | T1016 | Sugiyama | UBA1 A1S9T UBE1 | MLYSFFMPAAKLKERLDQPMtEIVsRVSKRKLGRHVRALVL |
| P22392 | T94 | EPSD|PSP | NME2 NM23B | VAMVWEGLNVVKTGRVMLGEtNPADsKPGtIRGDFCIQVGR |
| P22626 | S225 | Sugiyama | HNRNPA2B1 HNRPA2B1 | GNFGFGDsRGGGGNFGPGPGsNFRGGsDGyGsGRGFGDGyN |
| P22626 | S231 | Sugiyama | HNRNPA2B1 HNRPA2B1 | DsRGGGGNFGPGPGsNFRGGsDGyGsGRGFGDGyNGyGGGP |
| P22626 | S259 | Sugiyama | HNRNPA2B1 HNRPA2B1 | GFGDGyNGyGGGPGGGNFGGsPGyGGGRGGYGGGGPGYGNQ |
| P23284 | T81 | Sugiyama | PPIB CYPB | IFGLFGKTVPKTVDNFVALAtGEKGFGYKNSKFHRVIKDFM |
| P23396 | S224 | Sugiyama | RPS3 OK/SW-cl.26 | LPDHVsIVEPKDEILPttPIsEQKGGKPEPPAMPQPVPtA_ |
| P23396 | T220 | Sugiyama | RPS3 OK/SW-cl.26 | PKKPLPDHVsIVEPKDEILPttPIsEQKGGKPEPPAMPQPV |
| P23396 | T221 | GPS6|SIGNOR|EPSD|PSP|Sugiyama | RPS3 OK/SW-cl.26 | KKPLPDHVsIVEPKDEILPttPIsEQKGGKPEPPAMPQPVP |
| P23396 | T242 | Sugiyama | RPS3 OK/SW-cl.26 | PIsEQKGGKPEPPAMPQPVPtA___________________ |
| P23443 | S394 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RPS6KB1 STK14A | QsEEDVsQFDSKFtRQtPVDsPDDstLsEsANQVFLGFtYV |
| P23443 | S434 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RPS6KB1 STK14A | VAPSVLESVKEKFsFEPKIRsPRRFIGsPRtPVsPVKFsPG |
| P23443 | S447 | GPS6|ELM|iPTMNet|EPSD|PSP | RPS6KB1 STK14A | sFEPKIRsPRRFIGsPRtPVsPVKFsPGDFWGRGASASTAN |
| P23443 | T444 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | RPS6KB1 STK14A | EKFsFEPKIRsPRRFIGsPRtPVsPVKFsPGDFWGRGASAS |
| P23526 | S183 | Sugiyama | AHCY SAHH | NLyKMMANGILKVPAINVNDsVtKsKFDNLyGCRESLIDGI |
| P23588 | S122 | Sugiyama | EIF4B | NLPyDVTEESIKEFFRGLNIsAVRLPREPsNPERLKGFGyA |
| P23769 | T176 | SIGNOR|EPSD|PSP | GATA2 | VASLTPTAAHSGSHLFGFPPtPPKEVsPDPSTTGAAsPASS |
| P23921 | S559 | Sugiyama | RRM1 RR1 | ALEASCDLAKEQGPyEtyEGsPVsKGILQYDMWNVTPTDLW |
| P24864 | S399 | PSP | CCNE1 CCNE | MLsEQNRAsPLPsGLLtPPQsGKKQSSGPEMA_________ |
| P24928 | S1920 | EPSD|PSP | POLR2A POLR2 | PVytPtsPKysPtsPtysPtsPKysPtsPtysPtsPKGstY |
| P24928 | S1934 | EPSD|PSP | POLR2A POLR2 | PtysPtsPKysPtsPtysPtsPKGstYsPtsPGYsPtsPTY |
| P24941 | T14 | Sugiyama | CDK2 CDKN2 | _______MENFQKVEKIGEGtyGVVyKARNKLTGEVVALKK |
| P24941 | Y15 | Sugiyama | CDK2 CDKN2 | ______MENFQKVEKIGEGtyGVVyKARNKLTGEVVALKKI |
| P24941 | Y19 | Sugiyama | CDK2 CDKN2 | __MENFQKVEKIGEGtyGVVyKARNKLTGEVVALKKIRLDt |
| P25054 | S1100 | Sugiyama | APC DP2.5 | ESTDDKHLKFQPHFGQQECVsPYRSRGANGSETNRVGSNHG |
| P25205 | T713 | Sugiyama | MCM3 | KTRQPDAKDGDsyDPyDFsDtEEEMPQVHtPKTADsQEtKE |
| P25786 | S14 | Sugiyama | PSMA1 HC2 NU PROS30 PSC2 | _______MFRNQyDNDVtVWsPQGRIHQIEYAMEAVKQGSA |
| P26358 | S154 | SIGNOR|EPSD|PSP | DNMT1 AIM CXXC9 DNMT | KPRTPRRsKsDGEAKPEPsPsPRITRKSTRQttITSHFAKG |
| P26368 | S79 | EPSD|PSP | U2AF2 U2AF65 | RRRSKPLTRGAKEEHGGLIRsPRHEKKKKVRKYWDVPPPGF |
| P26373 | S181 | Sugiyama | RPL13 BBC1 OK/SW-cl.46 | YKKEKARVItEEEKNFKAFAsLRMARANARLFGIRAKRAKE |
| P26373 | S77 | Sugiyama | RPL13 BBC1 OK/SW-cl.46 | PIVRCPTVRYHTKVRAGRGFsLEELRVAGIHKKVARTIGIs |
| P26373 | T148 | Sugiyama | RPL13 BBC1 OK/SW-cl.46 | PRKPSAPKKGDssAEELKLAtQLtGPVMPVRNVYKKEKARV |
| P26373 | T151 | Sugiyama | RPL13 BBC1 OK/SW-cl.46 | PSAPKKGDssAEELKLAtQLtGPVMPVRNVYKKEKARVItE |
| P27348 | S45 | Sugiyama | YWHAQ | CMKAVtEQGAELsNEERNLLsVAyKNVVGGRRSAWRVIsSI |
| P27797 | S52 | Sugiyama | CALR CRTC | GWtsRWIEsKHKSDFGKFVLssGKFyGDEEKDKGLQTSQDA |
| P27797 | T34 | Sugiyama | CALR CRTC | LAVAEPAVYFKEQFLDGDGWtsRWIEsKHKSDFGKFVLssG |
| P27816 | S280 | Sugiyama | MAP4 | LAKDMALATKTEVALAKDMEsPtKLDVtLAKDMQPSMESDM |
| P27816 | S696 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP|Sugiyama | MAP4 | PVVSGTGNDIttPPNKELPPsPEKKTKPLATTQPAKtstsK |
| P27816 | S787 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | MAP4 | PsKDVKPKPIADAKAPEKRAsPsKPAsAPASRSGSKSTQTV |
| P27816 | T282 | Sugiyama | MAP4 | KDMALATKTEVALAKDMEsPtKLDVtLAKDMQPSMESDMAL |
| P27816 | T892 | EPSD|PSP | MAP4 | tttLsGtAPAAGVVPSRVKAtPMPsRPsttPFIDKKPTSAK |
| P27816 | T901 | EPSD|PSP | MAP4 | AAGVVPSRVKAtPMPsRPsttPFIDKKPTSAKPssttPRLS |
| P27816 | T917 | EPSD|PSP | MAP4 | RPsttPFIDKKPTSAKPssttPRLSRLAtNtsAPDLKNVRs |
| P27824 | S583 | EPSD|PSP|Sugiyama | CANX | VsQEEEDRKPKAEEDEILNRsPRNRKPRRE___________ |
| P28066 | S16 | PSP | PSMA5 | _____MFLTRsEyDRGVNtFsPEGRLFQVEyAIEAIKLGST |
| P29401 | S295 | Sugiyama | TKT | ysQIQsKKKILAtPPQEDAPsVDIANIRMPsLPsyKVGDKI |
| P29401 | S548 | Sugiyama | TKT | NIRVLDPFTIKPLDRKLILDsARAtKGRILTVEDHYYEGGI |
| P29401 | T287 | Sugiyama | TKT | AEQIIQEIysQIQsKKKILAtPPQEDAPsVDIANIRMPsLP |
| P29590 | S518 | EPSD|PSP | PML MYL PP8675 RNF71 TRIM19 | EARLARssPEQPRPstsKAVsPPHLDGPPsPRsPVIGsEVF |
| P29692 | S133 | SIGNOR|EPSD|PSP|Sugiyama | EEF1D EF1D | NVLEKssPGHRAtAPQtQHVsPMRQVEPPAKKPAtPAEDDE |
| P29966 | S26 | Sugiyama | MARCKS MACS PRKCSL | SKTAAKGEAAAERPGEAAVAssPsKANGQENGHVKVNGDAs |
| P29966 | S27 | Sugiyama | MARCKS MACS PRKCSL | KTAAKGEAAAERPGEAAVAssPsKANGQENGHVKVNGDAsP |
| P29966 | T150 | Sugiyama | MARCKS MACS PRKCSL | AsstssPKAEDGAtPsPsNEtPKKKKKRFsFKKsFKLsGFs |
| P30041 | T44 | Sugiyama | PRDX6 AOP2 KIAA0106 | RFHDFLGDSWGILFSHPRDFtPVCttELGRAAKLAPEFAKR |
| P30048 | S237 | Sugiyama | PRDX3 AOP1 | KAFQYVETHGEVCPANWtPDsPtIKPsPAASKEYFQKVNQ_ |
| P30050 | S165 | Sugiyama | RPL12 | GRHPHDIIDDINsGAVECPAs____________________ |
| P30086 | T42 | Sugiyama | PEBP1 PBP PEBP | QHPLHVTYAGAAVDELGKVLtPtQVKNRPtsIsWDGLDsGK |
| P30101 | S443 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | LsKDPNIVIAKMDAtANDVPsPyEVRGFPtIyFsPANKKLN |
| P30101 | S456 | EPSD|PSP|Sugiyama | PDIA3 ERP57 ERP60 GRP58 | AtANDVPsPyEVRGFPtIyFsPANKKLNPKKyEGGRELsDF |
| P30260 | S222 | EPSD|PSP | CDC27 ANAPC3 D0S1430E D17S978E | LTEtPQDtIELNRLNLEssNsKYSLNTDSSVSYIDSAVISP |
| P30260 | S312 | EPSD|PSP | CDC27 ANAPC3 D0S1430E D17S978E | PGDGSYLQNYTNTPPVIDVPsTGAPSKKSVARIGQTGtKSV |
| P30260 | S364 | GPS6|ELM|iPTMNet|EPSD | CDC27 ANAPC3 D0S1430E D17S978E | PILAQtQssGPQtsttPQVLsPtItsPPNALPRRSsRLFts |
| P30260 | S426 | SIGNOR|EPSD|PSP | CDC27 ANAPC3 D0S1430E D17S978E | NRKTKSKTNKGGITQPNINDsLEItKLDssIIsEGKIStIt |
| P30260 | S434 | EPSD|PSP | CDC27 ANAPC3 D0S1430E D17S978E | NKGGITQPNINDsLEItKLDssIIsEGKIStItPQIQAFNL |
| P30260 | S435 | EPSD|PSP | CDC27 ANAPC3 D0S1430E D17S978E | KGGITQPNINDsLEItKLDssIIsEGKIStItPQIQAFNLQ |
| P30260 | T205 | GPS6|ELM|iPTMNet|EPSD|PSP | CDC27 ANAPC3 D0S1430E D17S978E | TTQVPNHsLSHRQPEtVLTEtPQDtIELNRLNLEssNsKYS |
| P30260 | T209 | EPSD|PSP | CDC27 ANAPC3 D0S1430E D17S978E | PNHsLSHRQPEtVLTEtPQDtIELNRLNLEssNsKYSLNTD |
| P30260 | T289 | GPS6|ELM|iPTMNet|EPSD|PSP | CDC27 ANAPC3 D0S1430E D17S978E | LGGPAALSPLTPSFGILPLEtPSPGDGSYLQNYTNTPPVID |
| P30260 | T329 | EPSD|PSP | CDC27 ANAPC3 D0S1430E D17S978E | DVPsTGAPSKKSVARIGQTGtKSVFSQsGNsREVtPILAQt |
| P30260 | T343 | GPS6|ELM|iPTMNet|EPSD|PSP | CDC27 ANAPC3 D0S1430E D17S978E | RIGQTGtKSVFSQsGNsREVtPILAQtQssGPQtsttPQVL |
| P30260 | T430 | EPSD|PSP | CDC27 ANAPC3 D0S1430E D17S978E | KSKTNKGGITQPNINDsLEItKLDssIIsEGKIStItPQIQ |
| P30260 | T446 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CDC27 ANAPC3 D0S1430E D17S978E | sLEItKLDssIIsEGKIStItPQIQAFNLQKAAAEGLMSLL |
| P30291 | S123 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | WEE1 | DEAGGGAEGDSWEEEGFGsSsPVKsPAAPyFLGssFsPVRC |
| P30291 | S139 | PSP | WEE1 | FGsSsPVKsPAAPyFLGssFsPVRCGGPGDAsPRGCGARRA |
| P30304 | S116 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CDC25A | ENLENPMRRIHsLPQKLLGCsPALKRSHsDSLDHDIFQLID |
| P30304 | S18 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CDC25A | ___MELGPEPPHRRRLLFACsPPPASQPVVKALFGASAAGG |
| P30304 | S283 | EPSD|PSP | CDC25A | sLCssSTRSVLKRPERsQEEsPPGSTKRRKsMsGASPKEST |
| P30305 | S160 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | CDC25B CDC25HU2 | RNEQFAIRRFQsMPVRLLGHsPVLRNItNsQAPDGRRKsEA |
| P30305 | S321 | SIGNOR|EPSD|PSP | CDC25B CDC25HU2 | LEKEEEKDLVMYSKCQRLFRsPsMPCSVIRPILKRLERPQD |
| P30305 | S50 | GPS6|PSP | CDC25B CDC25HU2 | PGLLLGSHGLLGsPVRAAASsPVttLtQtMHDLAGLGSETP |
| P30307 | S122 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CDC25C | SGLQEVHLAGMNHDQHLMKCsPAQLLCstPNGLDRGHRKRD |
| P30307 | S168 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CDC25C | SANKENDNGNLVDSEMKYLGsPITTVPKLDKNPNLGEDQAE |
| P30307 | S214 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CDC25C | LMEFsLKDQEAKVSRsGLYRsPsMPENLNRPRLKQVEKFKD |
| P30307 | T130 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CDC25C | AGMNHDQHLMKCsPAQLLCstPNGLDRGHRKRDAMCSSSAN |
| P30307 | T48 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CDC25C | MLNLLLERDTsFTVCPDVPRtPVGKFLGDSANLsILsGGtP |
| P30307 | T67 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CDC25C | RtPVGKFLGDSANLsILsGGtPKRCLDLsNLSSGEITATQL |
| P30622 | T287 | SIGNOR | CLIP1 CYLN1 RSN | PKyGLFAPVHKVTKIGFPsttPAKAKANAVRRVMATtsAsL |
| P31350 | S20 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RRM2 RR2 | _MLSLRVPLAPItDPQQLQLsPLKGLsLVDKENtPPALsGT |
| P31350 | T33 | SIGNOR|EPSD|PSP | RRM2 RR2 | DPQQLQLsPLKGLsLVDKENtPPALsGTRVLASKTARRIFQ |
| P31749 | S473 | PSP | AKT1 PKB RAC | DQDDSMECVDSERRPHFPQFsysAsGtA_____________ |
| P31749 | T308 | PSP | AKT1 PKB RAC | IKITDFGLCKEGIKDGAtMKtFCGtPEyLAPEVLEDNDyGR |
| P31943 | S104 | Sugiyama | HNRNPH1 HNRPH HNRPH1 | EVFKSNNVEMDWVLKHtGPNsPDtANDGFVRLRGLPFGCSK |
| P31943 | T100 | Sugiyama | HNRNPH1 HNRPH HNRPH1 | HRyVEVFKSNNVEMDWVLKHtGPNsPDtANDGFVRLRGLPF |
| P31946 | S47 | Sugiyama | YWHAB | AMKAVtEQGHELsNEERNLLsVAyKNVVGARRSsWRVIsSI |
| P31947 | S45 | Sugiyama | SFN HME1 | FMKGAVEKGEELsCEERNLLsVAyKNVVGGQRAAWRVLSsI |
| P31948 | S189 | SIGNOR | STIP1 | KLQDPRIMTTLSVLLGVDLGsMDEEEEIAtPPPPPPPKKET |
| P31948 | S481 | Sugiyama | STIP1 | CKEAADGYQRCMMAQyNRHDsPEDVKRRAMADPEVQQIMSD |
| P31948 | T198 | SIGNOR | STIP1 | TLSVLLGVDLGsMDEEEEIAtPPPPPPPKKETKPEPMEEDL |
| P31948 | T332 | SIGNOR | STIP1 | KEEKYKDAIHFyNKSLAEHRtPDVLKKCQQAEKILKEQERL |
| P33316 | S99 | EPSD|PSP|Sugiyama | DUT | KGELPKAGGsPAPGPEtPAIsPsKRARPAEVGGMQLRFARL |
| P33908 | S12 | PSP | MAN1A1 | _________MPVGGLLPLFssPAGGVLGGGLGGGGGRKGSG |
| P33981 | S281 | PSP | TTK MPS1 MPS1L1 | QTNKTKQSCPFGRVPVNLLNsPDCDVKtDDsVVPCFMKRQT |
| P33991 | S32 | iPTMNet | MCM4 CDC21 | GSRRGRAtPAQtPRsEDARssPsQRRRGEDSTSTGELQPMP |
| P33991 | S88 | iPTMNet | MCM4 CDC21 | LFSsPPQMHSSAIPLDFDVSsPLTYGTPSSRVEGTPRSGVR |
| P33991 | T110 | iPTMNet | MCM4 CDC21 | LTYGTPSSRVEGTPRSGVRGtPVRQRPDLGsAQKGLQVDLQ |
| P33991 | T19 | SIGNOR|iPTMNet | MCM4 CDC21 | __MssPAstPSRRGSRRGRAtPAQtPRsEDARssPsQRRRG |
| P33991 | T7 | iPTMNet | MCM4 CDC21 | ______________MssPAstPSRRGSRRGRAtPAQtPRsE |
| P33993 | S121 | EPSD|PSP | MCM7 CDC47 MCM2 | VyIEHRLMMEQRSRDPGMVRsPQNQYPAELMRRFELYFQGP |
| P34897 | S266 | Sugiyama | SHMT2 | AHLLADMAHISGLVAAKVIPsPFKHADIVTtTTHKtLRGAR |
| P35251 | S518 | EPSD|PSP | RFC1 RFC140 | KKESKLERtPQKNVQGKRKIsPSKKESESKKSRPTSKRDSL |
| P35251 | T506 | SIGNOR|EPSD|PSP | RFC1 RFC140 | KSKYEIAVETEMKKESKLERtPQKNVQGKRKIsPSKKESES |
| P35611 | S12 | EPSD|PSP | ADD1 ADDA | _________MNGDsRAAVVtsPPPttAPHKERyFDRVDENN |
| P35611 | S355 | EPSD|PSP | ADD1 ADDA | AGGPDNLVLLNPEKYKAKsRsPGsPVGEGtGsPPKWQIGEQ |
| P35611 | S465 | Sugiyama | ADD1 ADDA | tRWLNSGRGDEASEEGQNGssPKsKTKWTKEDGHRtstsAV |
| P35998 | T193 | Sugiyama | PSMC2 MSS1 | TYSDVGGCKEQIEKLREVVEtPLLHPERFVNLGIEPPKGVL |
| P36578 | S295 | Sugiyama | RPL4 RPL1 | sNyNLPMHKMINtDLsRILKsPEIQRALRAPRKKIHRRVLK |
| P36578 | S365 | Sugiyama | RPL4 RPL1 | RNHKLRVDKAAAAAAALQAKsDEKAAVAGKKPVVGKKGKKA |
| P36956 | S439 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | SREBF1 BHLHD1 SREBP1 | TEVEDTLtPPPsDAGsPFQSsPLSLGSRGsGsGGsGsDsEP |
| P37802 | T180 | Sugiyama | TAGLN2 KIAA0120 CDABP0035 | RNFsDNQLQEGKNVIGLQMGtNRGAsQAGMtGyGMPRQIL_ |
| P38398 | S114 | PSP | BRCA1 RNF53 | QLDTGLEYANSYNFAKKENNsPEHLKDEVSIIQSMGYRNRA |
| P38398 | S1189 | SIGNOR|EPSD|PSP | BRCA1 RNF53 | DIKESsAVFSKsVQKGELsRsPsPFtHTHLAQGYRRGAKKL |
| P38398 | S1191 | SIGNOR|EPSD|PSP | BRCA1 RNF53 | KESsAVFSKsVQKGELsRsPsPFtHTHLAQGYRRGAKKLEs |
| P38398 | S1497 | SIGNOR|EPSD|PSP | BRCA1 RNF53 | FEVsADssTsKNKEPGVERssPSKCPsLDDRWYMHSCsGSL |
| P38919 | T163 | PSP | EIF4A3 DDX48 KIAA0111 | GTNVGEDIRKLDyGQHVVAGtPGRVFDMIRRRSLRTRAIKM |
| P38936 | S130 | EPSD|PSP | CDKN1A CAP20 CDKN1 CIP1 MDA6 PIC1 SDI1 WAF1 | HVDLsLSCTLVPRsGEQAEGsPGGPGDSQGRKRRQtsMTDF |
| P39019 | Y54 | Sugiyama | RPS19 | VDtVKLAKHKELAPyDENWFytRAAstARHLYLRGGAGVGs |
| P39023 | S13 | Sugiyama | RPL3 OK/SW-cl.32 | ________MSHRKFSAPRHGsLGFLPRKRSSRHRGKVKSFP |
| P39023 | S265 | Sugiyama | RPL3 OK/SW-cl.32 | HRGLRKVACIGAWHPARVAFsVARAGQKGYHHRTEINKKIY |
| P39748 | S187 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | FEN1 RAD2 | VKAGKVYAAATEDMDCLTFGsPVLMRHLtASEAKKLPIQEF |
| P39880 | S1237 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | CUX1 CUTL1 | VsDsQPCEPPsVGtEysQGAsPQPQHQLKKPRVVLAPEEKE |
| P39880 | S1270 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | CUX1 CUTL1 | VLAPEEKEALKRAYQQKPYPsPKTIEDLATQLNLKTSTVIN |
| P40337 | S80 | SIGNOR | VHL | RPVLRSVNsREPsQVIFCNRsPRVVLPVWLNFDGEPQPYPt |
| P40763 | S727 | GPS6 | STAT3 APRF | KTKFICVtPttCsNtIDLPMsPRTLDSLMQFGNNGEGAEPS |
| P42166 | S424 | EPSD|PSP | TMPO LAP2 | DVENIQKRIDQSKFQETEFLsPPRKVPRLSEKsVEERDsGs |
| P42695 | T1415 | PSP | NCAPD3 CAPD3 KIAA0056 | YSLEQESNGEIEHVTKRAIStPEKsISDVTFGAGVSYIGtP |
| P42892 | S733 | Sugiyama | ECE1 | VWCSVRTPESSHEGLITDPHsPsRFRVIGSLSNSKEFSEHF |
| P42898 | T34 | SIGNOR|PSP | MTHFR | CLEGSASSGSESSKDSSRCStPGLDPERHERLREKMRRRLE |
| P43307 | S268 | EPSD|PSP | SSR1 TRAPA PSEC0262 | QNDVDMsWIPQEtLNQINKAsPRRLPRKRAQKRSVGSDE__ |
| P46013 | T1943 | EPSD|PSP | MKI67 | tPVEKLDLLGNLPGsKRRPQtPKEKAKALEDLAGFKELFQt |
| P46013 | T761 | EPSD|PSP | MKI67 | ISNQKMDFKEDLSGIAEMFKtPVKEQPQLTSTCHIAISNSE |
| P46060 | S428 | SIGNOR | RANGAP1 KIAA1835 SD | AtPSRKILDPNTGEPAPVLssPPPADVstFLAFPsPEKLLR |
| P46060 | S442 | SIGNOR | RANGAP1 KIAA1835 SD | PAPVLssPPPADVstFLAFPsPEKLLRLGPKssVLIAQQTD |
| P46060 | T409 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RANGAP1 KIAA1835 SD | EEEEEEEEEPQQRGQGEKSAtPSRKILDPNTGEPAPVLssP |
| P46087 | S732 | Sugiyama | NOP2 NOL1 NSUN1 | AFLRQNAPPKGTDtQtPAVLsPsKtQAtLKPKDHHQPLGRA |
| P46527 | T187 | SIGNOR|PSP | CDKN1B KIP1 p27 | ANRTEENVsDGsPNAGSVEQtPKKPGLRRRQt_________ |
| P46531 | S2513 | GPS6 | NOTCH1 TAN1 | PVDNTPSHQLQVPEHPFLtPsPEsPDQWssssPHSNVSDWS |
| P46531 | S2516 | GPS6 | NOTCH1 TAN1 | NTPSHQLQVPEHPFLtPsPEsPDQWssssPHSNVSDWSEGV |
| P46777 | S172 | Sugiyama | RPL5 MSTP030 | RTTTGNKVFGALKGAVDGGLsIPHstKRFPGyDsEsKEFNA |
| P46777 | S176 | Sugiyama | RPL5 MSTP030 | GNKVFGALKGAVDGGLsIPHstKRFPGyDsEsKEFNAEVHR |
| P46782 | S142 | Sugiyama | RPS5 | REDSTRIGRAGTVRRQAVDVsPLRRVNQAIWLLCTGAREAA |
| P46937 | S128 | PSP | YAP1 YAP65 | AstDAGtAGALtPQHVRAHssPAsLQLGAVsPGtLtPtGVV |
| P46937 | S138 | SIGNOR|EPSD|PSP | YAP1 YAP65 | LtPQHVRAHssPAsLQLGAVsPGtLtPtGVVsGPAAtPTAQ |
| P46937 | S217 | PSP | YAP1 YAP65 | TTWQDPRKAMLSQMNVTAPTsPPVQQNMMNsASGPLPDGWE |
| P46937 | S289 | EPSD|PSP | YAP1 YAP65 | MNQRIsQsAPVKQPPPLAPQsPQGGVMGGsNsNQQQQMRLQ |
| P46937 | S367 | SIGNOR|EPSD|PSP | YAP1 YAP65 | ALRSQLPtLEQDGGtQNPVssPGMsQELRTMttNssDPFLN |
| P46937 | T119 | EPSD|PSP | YAP1 YAP65 | PEPKsHsRQAstDAGtAGALtPQHVRAHssPAsLQLGAVsP |
| P46937 | T143 | SIGNOR|EPSD|PSP | YAP1 YAP65 | VRAHssPAsLQLGAVsPGtLtPtGVVsGPAAtPTAQHLRQs |
| P47736 | S484 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RAP1GAP KIAA0474 RAP1GA1 | APNNPDLAKAAGIsLIVPGKsPtRKKsGPFGsRRssAIGIE |
| P47756 | S207 | Sugiyama | CAPZB | MNLGGsLtRQMEKDEtVsDCsPHIANIGRLVEDMENKIRst |
| P47914 | S142 | Sugiyama | RPL29 | KAKAKAKAKDQTKAQAAAPAsVPAQAPKRtQAPtKAsE___ |
| P48200 | S157 | SIGNOR|ELM|iPTMNet|EPSD|PSP | IREB2 | CAIQNAPNPGGGDLQKAGKLsPLKVQPKKLPCRGQTTCRGs |
| P48637 | S415 | Sugiyama | GSS | yILMEKIEPEPFENCLLRPGsPARVVQCISELGIFGVYVRQ |
| P48681 | T1299 | ELM | NES Nbla00170 | GEEsREEsEEDELGETLPDStPLGFYLRsPtsPRWDPTGEQ |
| P48681 | T315 | ELM|iPTMNet | NES Nbla00170 | LSLEVATYRTLLEAENsRLQtPGGGsKtsLsFQDPKLELQF |
| P48739 | S165 | Sugiyama | PITPNB | DRSQVEPADyKADEDPALFQsVKtKRGPLGPNWKKELANsP |
| P49006 | S22 | Sugiyama | MARCKSL1 MLP MRP | GSQSSKAPRGDVtAEEAAGAsPAKANGQENGHVKsNGDLsP |
| P49418 | S272 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | AMPH AMPH1 | SGPLRIAKtPsPPEEPsPLPsPtAsPNHTLAPAsPAPARPR |
| P49418 | S276 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | AMPH AMPH1 | RIAKtPsPPEEPsPLPsPtAsPNHTLAPAsPAPARPRsPsQ |
| P49418 | S285 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | AMPH AMPH1 | EEPsPLPsPtAsPNHTLAPAsPAPARPRsPsQTRKGPPVPP |
| P49450 | S68 | SIGNOR|EPSD|PSP | CENPA | LKEIRKLQKSTHLLIRKLPFsRLAREICVKFTRGVDFNWQA |
| P49454 | T144 | Sugiyama | CENPF | ELERSQQAAQSADVSLNPCNtPQKIFTTPLtPsQYYSGSKY |
| P49459 | S120 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | UBE2A RAD6A | YDVSSILTSIQSLLDEPNPNsPANSQAAQLYQENKREYEKR |
| P49736 | S13 | GPS6 | MCM2 BM28 CCNL1 CDCL1 KIAA0030 | ________MAEssEsFtMAssPAQRRRGNDPLtssPGRssR |
| P49736 | S27 | GPS6|Sugiyama | MCM2 BM28 CCNL1 CDCL1 KIAA0030 | sFtMAssPAQRRRGNDPLtssPGRssRRtDALtssPGRDLP |
| P49736 | S41 | GPS6 | MCM2 BM28 CCNL1 CDCL1 KIAA0030 | NDPLtssPGRssRRtDALtssPGRDLPPFEDEsEGLLGtEG |
| P49768 | T354 | ELM | PSEN1 AD3 PS1 PSNL1 | GGFsEEWEAQRDsHLGPHRstPEsRAAVQELsssILAGEDP |
| P49792 | S2246 | SIGNOR|EPSD|PSP | RANBP2 NUP358 | NYDLREDALDDsVssssVHAsPLAssPVRKNLFRFGEsttG |
| P49792 | S2251 | SIGNOR|EPSD|PSP | RANBP2 NUP358 | EDALDDsVssssVHAsPLAssPVRKNLFRFGEsttGFNFsF |
| P49792 | S2276 | SIGNOR|EPSD|PSP | RANBP2 NUP358 | NLFRFGEsttGFNFsFKsALsPsKsPAKLNQsGtsVGtDEE |
| P49792 | S2280 | SIGNOR|EPSD|PSP | RANBP2 NUP358 | FGEsttGFNFsFKsALsPsKsPAKLNQsGtsVGtDEEsDVt |
| P49792 | T2153 | SIGNOR|EPSD|PSP | RANBP2 NUP358 | EEFKQKFEECQRLLLDIPLQtPHKLVDtGRAAKLIQRAEEM |
| P49821 | T383 | SIGNOR|PSP | NDUFV1 UQOR1 | IVKAIARLIEFYKHESCGQCtPCREGVDWMNKVMARFVRGD |
| P49915 | T318 | EPSD|PSP | GMPS | NAAHSFYNGtttLPIsDEDRtPRKRISKTLNMttsPEEKRK |
| P49916 | S210 | EPSD|PSP | LIG3 | GtPKKKAVVQAKLtttGQVtsPVKGAsFVTSTNPRKFsGFs |
| P49916 | S913 | EPSD|PSP | LIG3 | NMQTAKPSAMKVGEKLAtKssPVKVGEKRKAADETLCQTKV |
| P49916 | T191 | EPSD|PSP | LIG3 | DNEKEQITQHIADLSSKAAGtPKKKAVVQAKLtttGQVtsP |
| P50502 | S181 | Sugiyama | ST13 AAG2 FAM10A1 HIP SNC6 | LQKPNAAIRDCDRAIEINPDsAQPyKWRGKAHRLLGHWEEA |
| P50570 | S764 | EPSD|PSP | DNM2 DYN2 | VstPVPPPVDDtWLQsAssHsPtPQRRPVSSIHPPGRPPAV |
| P50570 | T766 | EPSD|PSP | DNM2 DYN2 | tPVPPPVDDtWLQsAssHsPtPQRRPVSSIHPPGRPPAVRG |
| P50613 | S164 | GPS6|iPTMNet|EPSD|PSP | CDK7 CAK CAK1 CDKN7 MO15 STK1 | LLDENGVLKLADFGLAKsFGsPNRAytHQVVtRWYRAPELL |
| P50613 | T170 | iPTMNet|EPSD|PSP | CDK7 CAK CAK1 CDKN7 MO15 STK1 | VLKLADFGLAKsFGsPNRAytHQVVtRWYRAPELLFGARMY |
| P50914 | S139 | Sugiyama | RPL14 | RNRIIKNEVKKLQKAALLKAsPKKAPGTKGTAAAAAAAAAA |
| P50993 | S719 | Sugiyama | ATP1A2 KIAA0778 | VEGCQRQGAIVAVTGDGVNDsPALKKADIGIAMGISGSDVS |
| P51003 | S537 | SIGNOR | PAPOLA PAP | ALNDSSLDLsMDsDNsMsVPsPtSATKtsPLNSSGsSQGRN |
| P51003 | S545 | SIGNOR | PAPOLA PAP | LsMDsDNsMsVPsPtSATKtsPLNSSGsSQGRNsPAPAVTA |
| P51003 | S558 | SIGNOR | PAPOLA PAP | PtSATKtsPLNSSGsSQGRNsPAPAVTAASVTNIQATEVSV |
| P51587 | S3291 | GPS6|EPSD|PSP | BRCA2 FACD FANCD1 | LDFLSRLPLPPPVSPICTFVsPAAQKAFQPPRSCGTKYETP |
| P51858 | S165 | Sugiyama | HDGF HMG1L2 | AKEKNEKGALKRRAGDLLEDsPKRPKEAENPEGEEKEAAtL |
| P51991 | S358 | Sugiyama | HNRNPA3 HNRPA3 | QQQSNYGPMKGGsFGGRssGsPyGGGyGsGGGsGGyGsRRF |
| P52292 | S62 | PSP | KPNA2 RCH1 SRP1 | KKDDQMLKRRNVssFPDDAtsPLQENRNNQGtVNWSVDDIV |
| P52292 | T9 | PSP | KPNA2 RCH1 SRP1 | ____________MstNENANtPAARLHRFKNKGKDsTEMRR |
| P52597 | S203 | Sugiyama | HNRNPF HNRPF | VFKssQEEVRsysDPPLKFMsVQRPGPYDRPGtARRyIGIV |
| P52701 | S292 | Sugiyama | MSH6 GTBP | EGssDEIssGVGDsESEGLNsPVKVARKRKRMVTGNGsLKR |
| P52732 | T926 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | KIF11 EG5 KNSL1 TRIP5 | LTKLNCFLEQDLKLDIPtGttPQRKsyLyPSTLVRTEPREH |
| P52789 | S415 | Sugiyama | HK2 | QRIKENKGEERLRstIGVDGsVyKKHPHFAKRLHKTVRRLV |
| P52926 | S44 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | HMGA2 HMGIC | PQKRGRGRPRKQQQEPtGEPsPKRPRGRPKGSKNKsPSKAA |
| P52926 | S59 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | HMGA2 HMGIC | PtGEPsPKRPRGRPKGSKNKsPSKAAQKKAEATGEKRPRGR |
| P52948 | S612 | SIGNOR | NUP98 ADAR2 | MPKKsIKKLVLKNLNNsNLFsPVNRDsENLAsPsEyPENGE |
| P52948 | S623 | SIGNOR | NUP98 ADAR2 | KNLNNsNLFsPVNRDsENLAsPsEyPENGERFsFLSKPVDE |
| P52948 | T670 | SIGNOR | NUP98 ADAR2 | DEDsLVsHFytNPIAKPIPQtPEsAGNKHsNsNsVDDtIVA |
| P54132 | S714 | EPSD|PSP | BLM RECQ2 RECQL3 | GKSLCYQLPACVSPGVTVVIsPLRSLIVDQVQKLTSLDIPA |
| P54132 | T766 | EPSD|PSP | BLM RECQ2 RECQL3 | ATNIYLQLSKKDPIIKLLYVtPEKICASNRLISTLENLYER |
| P54274 | T344 | GPS6|EPSD|PSP | TERF1 PIN2 TRBF1 TRF TRF1 | SKLQHGTQQQDLNKKERRVGtPQSTKKKKESRRAtESRIPV |
| P54274 | T371 | GPS6|EPSD|PSP | TERF1 PIN2 TRBF1 TRF TRF1 | KKESRRAtESRIPVSKsQPVtPEKHRARKRQAWLWEEDKNL |
| P54578 | T235 | EPSD|PSP | USP14 TGT | LEAIEDDsVKETDsssAsAAtPSKKKSLIDQFFGVEFETTM |
| P55081 | T267 | Sugiyama | MFAP1 | ETKKELEENKRsLAALDALNtDDENDEEEyEAWKVRELKRI |
| P55211 | T125 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CASP9 MCH6 | NLtPVVLRPEIRKPEVLRPEtPRPVDIGSGGFGDVGALEsL |
| P55273 | S76 | EPSD|PSP | CDKN2D | IALELLKQGAsPNVQDTSGTsPVHDAARTGFLDTLKVLVEH |
| P55795 | S104 | Sugiyama | HNRNPH2 FTP3 HNRPH2 | EVFKSNsVEMDWVLKHtGPNsPDtANDGFVRLRGLPFGCSK |
| P55795 | T100 | Sugiyama | HNRNPH2 FTP3 HNRPH2 | HRyVEVFKSNsVEMDWVLKHtGPNsPDtANDGFVRLRGLPF |
| P55809 | S509 | Sugiyama | OXCT1 OXCT SCOT | LWEGLTVDDVQKSTGCDFAVsPKLMPMQQIAN_________ |
| P56181 | S105 | SIGNOR|PSP | NDUFV3 | LDLNLELSKFRMPQPssGREsPRH_________________ |
| P60709 | S323 | Sugiyama | ACTB | ttMyPGIADRMQKEItALAPstMKIKIIAPPERKYsVWIGG |
| P60709 | T106 | Sugiyama | ACTB | WHHtFyNELRVAPEEHPVLLtEAPLNPKANREKMTQIMFET |
| P60709 | T324 | Sugiyama | ACTB | tMyPGIADRMQKEItALAPstMKIKIIAPPERKYsVWIGGs |
| P60866 | T6 | Sugiyama | RPS20 | _______________MAFKDtGKtPVEPEVAIHRIRITLTS |
| P60891 | S103 | SIGNOR|PSP | PRPS1 | SRVTAVIPCFPYARQDKKDKsRAPISAKLVANMLSVAGADH |
| P61020 | S123 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RAB5B | TNQETFARAKTWVKELQRQAsPsIVIALAGNKADLANKRMV |
| P61254 | S32 | Sugiyama | RPL26 | sKNRKRHFNAPsHIRRKIMssPLSKELRQKYNVRSMPIRKD |
| P61254 | T8 | Sugiyama | RPL26 | _____________MKFNPFVtsDRsKNRKRHFNAPsHIRRK |
| P61353 | T94 | Sugiyama | RPL27 | VyNyNHLMPtRysVDIPLDKtVVNKDVFRDPALKRKARREA |
| P61371 | S269 | PSP | ISL1 | QQPNDKTNIQGMtGtPMVAAsPERHDGGLQANPVEVQSYQP |
| P61604 | S64 | Sugiyama | HSPE1 | AtVVAVGsGsKGKGGEIQPVsVKVGDKVLLPEyGGtKVVLD |
| P61916 | S40 | Sugiyama | NPC2 HE1 | EPVQFKDCGsVDGVIKEVNVsPCPtQPCQLSKGQSYSVNVT |
| P61978 | S216 | EPSD|PSP | HNRNPK HNRPK | GGKPDRVVECIKIILDLIsEsPIKGRAQPyDPNFyDETyDy |
| P61978 | S284 | Sugiyama | HNRNPK HNRPK | MPPGRGGRPMPPSRRDyDDMsPRRGPPPPPPGRGGRGGsRA |
| P61981 | S46 | Sugiyama | YWHAG | AMKNVtELNEPLsNEERNLLsVAyKNVVGARRSsWRVIsSI |
| P62136 | T320 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | PPP1CA PPP1A | DKNKGKyGQFSGLNPGGRPItPPRNsAKAKK__________ |
| P62195 | T109 | Sugiyama | PSMC5 SUG1 | VHPEGKFVVDVDKNIDINDVtPNCRVALRNDsytLHKILPN |
| P62249 | S9 | Sugiyama | RPS16 | ____________MPsKGPLQsVQVFGRKKTATAVAHCKRGN |
| P62258 | S46 | Sugiyama | YWHAE | SMKKVAGMDVELTVEERNLLsVAyKNVIGARRASWRIIssI |
| P62263 | S114 | Sugiyama | RPS14 PRO2640 | HIKLRATGGNRtKtPGPGAQsALRALARSGMKIGRIEDVtP |
| P62263 | S139 | Sugiyama | RPS14 PRO2640 | LARSGMKIGRIEDVtPIPsDstRRKGGRRGRRL________ |
| P62263 | T107 | Sugiyama | RPS14 PRO2640 | ELGITALHIKLRATGGNRtKtPGPGAQsALRALARSGMKIG |
| P62263 | T133 | Sugiyama | RPS14 PRO2640 | QsALRALARSGMKIGRIEDVtPIPsDstRRKGGRRGRRL__ |
| P62266 | T34 | Sugiyama | RPS23 | RSHRRDQKWHDKQYKKAHLGtALKANPFGGAsHAKGIVLEK |
| P62277 | S14 | Sugiyama | RPS13 | _______MGRMHAPGKGLsQsALPyRRsVPtWLKLTsDDVK |
| P62736 | S325 | Sugiyama | ACTA2 ACTSA ACTVS GIG46 | tTMYPGIADRMQKEItALAPstMKIKIIAPPERKYSVWIGG |
| P62736 | T326 | Sugiyama | ACTA2 ACTSA ACTVS GIG46 | TMYPGIADRMQKEItALAPstMKIKIIAPPERKYSVWIGGS |
| P62750 | S43 | Sugiyama | RPL23A | KAKKAVLKGVHSHKKKKIRtsPTFRRPKTLRLRRQPKYPRK |
| P62750 | T42 | Sugiyama | RPL23A | LKAKKAVLKGVHSHKKKKIRtsPTFRRPKTLRLRRQPKYPR |
| P62826 | T21 | Sugiyama | RAN ARA24 OK/SW-cl.81 | MAAQGEPQVQFKLVLVGDGGtGKttFVKRHLtGEFEKKyVA |
| P62826 | T66 | Sugiyama | RAN ARA24 OK/SW-cl.81 | EVHPLVFHTNRGPIKFNVWDtAGQEKFGGLRDGYYIQAQCA |
| P62899 | T119 | Sugiyama | RPL31 | PNKLytLVtyVPVttFKNLQtVNVDEN______________ |
| P62917 | S14 | Sugiyama | RPL8 | _______MGRVIRGQRKGAGsVFRAHVKHRKGAARLRAVDF |
| P62942 | S9 | Sugiyama | FKBP1A FKBP1 FKBP12 | ____________MGVQVEtIsPGDGRtFPKRGQtCVVHytG |
| P62942 | T7 | Sugiyama | FKBP1A FKBP1 FKBP12 | ______________MGVQVEtIsPGDGRtFPKRGQtCVVHy |
| P63104 | S28 | Sugiyama | YWHAZ | QKAKLAEQAERyDDMAACMKsVtEQGAELsNEERNLLsVAy |
| P63104 | S45 | Sugiyama | YWHAZ | CMKsVtEQGAELsNEERNLLsVAyKNVVGARRssWRVVssI |
| P63173 | T14 | Sugiyama | RPL38 | _______MPRKIEEIKDFLLtARRKDAKSVKIKKNKDNVKF |
| P63261 | S323 | Sugiyama | ACTG1 ACTG | ttMyPGIADRMQKEItALAPstMKIKIIAPPERKYsVWIGG |
| P63261 | T106 | Sugiyama | ACTG1 ACTG | WHHtFyNELRVAPEEHPVLLtEAPLNPKANREKMTQIMFET |
| P63261 | T324 | Sugiyama | ACTG1 ACTG | tMyPGIADRMQKEItALAPstMKIKIIAPPERKYsVWIGGs |
| P63267 | S324 | Sugiyama | ACTG2 ACTA3 ACTL3 ACTSG | tTMYPGIADRMQKEItALAPstMKIKIIAPPERKYSVWIGG |
| P63267 | T325 | Sugiyama | ACTG2 ACTA3 ACTL3 ACTSG | TMYPGIADRMQKEItALAPstMKIKIIAPPERKYSVWIGGS |
| P63279 | S71 | EPSD|PSP | UBE2I UBC9 UBCE9 | TPWEGGLFKLRMLFKDDYPssPPKCKFEPPLFHPNVYPSGT |
| P67775 | T304 | GPS6|PSP | PPP2CA | ySFLQFDPAPRRGEPHVTRRtPDyFL_______________ |
| P67809 | S102 | Sugiyama | YBX1 NSEP1 YB1 | EDVFVHQtAIKKNNPRKyLRsVGDGEtVEFDVVEGEKGAEA |
| P67809 | T89 | Sugiyama | YBX1 NSEP1 YB1 | RNGyGFINRNDtKEDVFVHQtAIKKNNPRKyLRsVGDGEtV |
| P67870 | S209 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CSNK2B CK2N G5A | GFKIHPMAYQLQLQAAsNFKsPVKtIR______________ |
| P68032 | S325 | Sugiyama | ACTC1 ACTC | tTMYPGIADRMQKEItALAPstMKIKIIAPPERKYSVWIGG |
| P68032 | T326 | Sugiyama | ACTC1 ACTC | TMYPGIADRMQKEItALAPstMKIKIIAPPERKYSVWIGGS |
| P68133 | S325 | Sugiyama | ACTA1 ACTA | TTMYPGIADRMQKEItALAPstMKIKIIAPPERKYSVWIGG |
| P68133 | T326 | Sugiyama | ACTA1 ACTA | TMYPGIADRMQKEItALAPstMKIKIIAPPERKYSVWIGGS |
| P68363 | T56 | Sugiyama | TUBA1B | MPSDKtIGGGDDsFNtFFsEtGAGKHVPRAVFVDLEPtVID |
| P68363 | T73 | Sugiyama | TUBA1B | FsEtGAGKHVPRAVFVDLEPtVIDEVRtGtyRQLFHPEQLI |
| P68363 | Y83 | Sugiyama | TUBA1B | PRAVFVDLEPtVIDEVRtGtyRQLFHPEQLItGKEDAANNy |
| P68400 | S362 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CSNK2A1 CK2A1 | GStPVSSANMMSGISSVPtPsPLGPLAGsPVIAAANPLGMP |
| P68400 | S370 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CSNK2A1 CK2A1 | NMMSGISSVPtPsPLGPLAGsPVIAAANPLGMPVPAAAGAQ |
| P68400 | T344 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CSNK2A1 CK2A1 | FytVVKDQARMGSSSMPGGStPVSSANMMSGISSVPtPsPL |
| P68400 | T360 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CSNK2A1 CK2A1 | PGGStPVSSANMMSGISSVPtPsPLGPLAGsPVIAAANPLG |
| P78316 | S96 | Sugiyama | NOP14 C4orf9 NOL14 RES4-25 | ERDKSNVFRDKRFGEyNsNMsPEEKMMKRFALEQQRHHEKK |
| P78344 | T508 | SIGNOR|EPSD|PSP | EIF4G2 DAP5 OK/SW-cl.75 | PKLQPQITMIPPsAQPPRtQtPPLGQtPQLGLKTNPPLIQE |
| P78347 | S210 | Sugiyama | GTF2I BAP135 WBSCR6 | EPKKHVGGRVMVtDADRsILsPGGsCGPIKVKTEPTEDSGI |
| P82970 | T31 | EPSD|PSP | HMGN5 NSBP1 | DMRQEPKRRsARLsAMLVPVtPEVKPKRTSSSRKMKTKSDM |
| P83731 | S38 | Sugiyama | RPL24 | GRRYARTDGKVFQFLNAKCEsAFLSKRNPRQINWtVLyRRK |
| P83731 | S9 | Sugiyama | RPL24 | ____________MKVELCsFsGyKIYPGHGRRYARTDGKVF |
| P83731 | T52 | Sugiyama | RPL24 | LNAKCEsAFLSKRNPRQINWtVLyRRKHKKGQsEEIQKKRT |
| P83731 | Y55 | Sugiyama | RPL24 | KCEsAFLSKRNPRQINWtVLyRRKHKKGQsEEIQKKRTRRA |
| P84098 | S13 | Sugiyama | RPL19 | ________MSMLRLQKRLAssVLRCGKKKVWLDPNEtNEIA |
| P84098 | S37 | Sugiyama | RPL19 | CGKKKVWLDPNEtNEIANANsRQQIRKLIKDGLIIRKPVtV |
| P85037 | S420 | Sugiyama | FOXK1 MNF | RGVSCFRtPFGPLssRsAPAsPtHPGLMsPRsGGLQtPECL |
| P85037 | S428 | Sugiyama | FOXK1 MNF | PFGPLssRsAPAsPtHPGLMsPRsGGLQtPECLsREGsPIP |
| P98170 | S40 | EPSD|PSP | XIAP API3 BIRC4 IAP3 | EEEFVEEFNRLKTFANFPsGsPVSASTLARAGFLYTGEGDT |
| Q00526 | T14 | Sugiyama | CDK3 CDKN3 | _______MDMFQKVEKIGEGtyGVVyKAKNRETGQLVALKK |
| Q00526 | Y15 | Sugiyama | CDK3 CDKN3 | ______MDMFQKVEKIGEGtyGVVyKAKNRETGQLVALKKI |
| Q00526 | Y19 | Sugiyama | CDK3 CDKN3 | __MDMFQKVEKIGEGtyGVVyKAKNRETGQLVALKKIRLDL |
| Q00536 | S95 | ELM | CDK16 PCTAIRE1 PCTK1 | KMGsDGEsDQAsAtssDEVQsPVRVRMRNHPPRKIstEDIN |
| Q01094 | S332 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | E2F1 RBBP3 | PSQEVTSEEENRAtDsAtIVsPPPssPPssLttDPSQSLLS |
| Q01094 | S337 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | E2F1 RBBP3 | TSEEENRAtDsAtIVsPPPssPPssLttDPSQSLLSLEQEP |
| Q01105 | S161 | Sugiyama | SET | FDENPyFENKVLSKEFHLNEsGDPssKstEIKWKSGKDLTK |
| Q01105 | S7 | GPS6|PSP | SET | ______________MAPKRQsPLPPQKKKPRPPPALGPEEt |
| Q01105 | T169 | Sugiyama | SET | NKVLSKEFHLNEsGDPssKstEIKWKSGKDLTKRssQTQNK |
| Q01130 | S212 | Sugiyama | SRSF2 SFRS2 | PPPVsKRESKSRSRsKsPPKsPEEEGAVss___________ |
| Q01167 | S373 | SIGNOR|EPSD|PSP | FOXK2 ILF ILF1 | RGVPCFRtPLGPLssRsAPAsPNHAGVLsAHssGAQtPEsL |
| Q01167 | S428 | SIGNOR|EPSD|PSP | FOXK2 ILF ILF1 | AAQPKLAVIQEARFAQsAPGsPLssQPVLITVQRQLPQAIK |
| Q01196 | S21 | SIGNOR | RUNX1 AML1 CBFA2 | MRIPVDASTSRRFtPPstALsPGKMsEALPLGAPDAGAALA |
| Q01196 | S249 | SIGNOR | RUNX1 AML1 CBFA2 | stAFNPQPQSQMQDTRQIQPsPPWsyDQsyQyLGSIAsPsV |
| Q01196 | S266 | SIGNOR | RUNX1 AML1 CBFA2 | IQPsPPWsyDQsyQyLGSIAsPsVHPAtPIsPGRASGMTTL |
| Q01196 | S276 | SIGNOR | RUNX1 AML1 CBFA2 | QsyQyLGSIAsPsVHPAtPIsPGRASGMTTLSAELSSRLsT |
| Q01196 | S397 | SIGNOR | RUNX1 AML1 CBFA2 | HLYYGASAGSYQFSMVGGERsPPRILPPCTNASTGSALLNP |
| Q01196 | T273 | SIGNOR | RUNX1 AML1 CBFA2 | syDQsyQyLGSIAsPsVHPAtPIsPGRASGMTTLSAELSSR |
| Q01581 | S495 | EPSD|PSP | HMGCS1 HMGCS | DtLDEGVGLVHsNIAtEHIPsPAKKVPRLPAtAAEPEAAVI |
| Q01814 | S1234 | Sugiyama | ATP2B2 PMCA2 | DSGINLTTDtsKSATSSsPGsPIHSLEtsL___________ |
| Q02363 | S5 | PSP | ID2 BHLHB26 | ________________MKAFsPVRSVRKNsLSDHSLGISRs |
| Q02539 | T4 | iPTMNet | H1-1 H1F1 HIST1H1A | _________________MsEtVPPAPAASAAPEKPLAGKKA |
| Q02750 | T286 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | MAP2K1 MEK1 PRKMK1 | PDAKELELMFGCQVEGDAAEtPPRPRtPGRPLssyGMDsRP |
| Q02750 | T292 | SIGNOR|EPSD|PSP | MAP2K1 MEK1 PRKMK1 | ELMFGCQVEGDAAEtPPRPRtPGRPLssyGMDsRPPMAIFE |
| Q02880 | S1424 | EPSD|PSP | TOP2B | NDGEDEFVPsDGLDKDEytFsPGKSKAtPEKsLHDKKsQDF |
| Q02952 | T618 | PSP | AKAP12 AKAP250 | sDGEKKREGVtPWAsFKKMVtPKKRVRRPsEsDKEDELDKV |
| Q02952 | T767 | SIGNOR|EPSD|PSP | AKAP12 AKAP250 | AGsPTEGEGVstWEsFKRLVtPRKKsKSKLEEKsEDsIAGs |
| Q03060 | S271 | SIGNOR|PSP | CREM | PTYQIRAPTAALPQGVVMAAsPGSLHsPQQLAEEATRKREL |
| Q03060 | S277 | SIGNOR|PSP | CREM | APTAALPQGVVMAAsPGSLHsPQQLAEEATRKRELRLMKNR |
| Q03188 | T734 | PSP | CENPC CENPC1 ICEN7 | KQSKVIPKNRIHHKLVLPsNtPNVRRTKRTRLKPLEYWRGE |
| Q03468 | T1031 | PSP | ERCC6 CSB | DASQSTETSAIFAGTGSDVQtPKCHLKRRIQPAFGADHDVP |
| Q04637 | S1231 | EPSD|PSP|Sugiyama | EIF4G1 EIF4F EIF4G EIF4GI | tEDRDRGRDAVKREAALPPVsPLKAALsEEELEKKsKAIIE |
| Q04917 | S46 | Sugiyama | YWHAH YWHA1 | AMKAVtELNEPLsNEDRNLLsVAyKNVVGARRSsWRVIsSI |
| Q05193 | S774 | ELM | DNM1 DNM | MPPPVDDSWLQVQSVPAGRRsPTSsPtPQRRAPAVPPARPG |
| Q05193 | S778 | ELM | DNM1 DNM | VDDSWLQVQSVPAGRRsPTSsPtPQRRAPAVPPARPGsRGP |
| Q05D32 | S104 | PSP | CTDSPL2 HSPC058 HSPC129 | tstPRAGEKPNKQISRVRRKsQVNGEAGsYEMTNQHVKQNG |
| Q05D32 | S134 | PSP | CTDSPL2 HSPC058 HSPC129 | EMTNQHVKQNGKLEDNPssGsPPRtTLLGtIFsPVFNFFSP |
| Q05D32 | T86 | PSP | CTDSPL2 HSPC058 HSPC129 | ENPSKRSRIERDIDNNLItstPRAGEKPNKQISRVRRKsQV |
| Q06413 | S396 | SIGNOR|EPSD|PSP | MEF2C | QSSNLSLPSTQsLNIKSEPVsPPRDRTTtPSRYPQHTRHEA |
| Q06481 | T736 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | APLP2 APPL2 | LRKRQYGtISHGIVEVDPMLtPEERHLNKMQNHGyENPtyK |
| Q06830 | S32 | Sugiyama | PRDX1 PAGA PAGB TDPX2 | APNFKAtAVMPDGQFKDIsLsDyKGKYVVFFFYPLDFTFVC |
| Q06830 | T90 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | PRDX1 PAGA PAGB TDPX2 | NCQVIGASVDSHFCHLAWVNtPKKQGGLGPMNIPLVSDPKR |
| Q07020 | S130 | Sugiyama | RPL18 | RSRILRAGGKILtFDQLALDsPKGCGtVLLsGPRKGREVYR |
| Q07021 | T165 | Sugiyama | C1QBP GC1QBP HABP1 SF2P32 | GEEEPSQGQKVEEQEPELtstPNFVVEVIKNDDGKKALVLD |
| Q07666 | T317 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | KHDRBS1 SAM68 | PPPVPRGRGVGPPRGALVRGtPVRGAITRGATVTRGVPPPP |
| Q07666 | T33 | PSP|Sugiyama | KHDRBS1 SAM68 | RssGRsGsMDPsGAHPsVRQtPsRQPPLPHRSRGGGGGSRG |
| Q07817 | S62 | GPS6|EPSD|PSP | BCL2L1 BCL2L BCLX | ESEMEtPsAINGNPSWHLADsPAVNGATGHSSSLDAREVIP |
| Q07820 | S64 | GPS6|EPSD|PSP | MCL1 BCL2L3 | ARREIGGGEAGAVIGGSAGAsPPstLtPDSRRVARPPPIGA |
| Q07820 | T92 | GPS6|SIGNOR|EPSD|PSP | MCL1 BCL2L3 | DSRRVARPPPIGAEVPDVTAtPARLLFFAPTRRAAPLEEME |
| Q07955 | S201 | Sugiyama | SRSF1 ASF SF2 SF2P33 SFRS1 OK/SW-cl.3 | RsHEGEtAyIRVKVDGPRsPsyGRsRsRsRsRsRsRsRsNs |
| Q07960 | S51 | Sugiyama | ARHGAP1 CDC42GAP RHOGAP1 | KNWPsDEMPDFPKsDDsKsssPELVtHLKWDDPyyDIARHQ |
| Q08050 | S251 | SIGNOR | FOXM1 FKHL16 HFH11 MPP2 WIN | NSVSERPPYSYMAMIQFAINstERKRMTLKDIYTWIEDHFP |
| Q08050 | S693 | GPS6|EPSD | FOXM1 FKHL16 HFH11 MPP2 WIN | PQRLLSSEPLDLIsVPFGNssPsDIDVPKPGsPEPQVsGLA |
| Q08050 | T600 | EPSD|PSP | FOXM1 FKHL16 HFH11 MPP2 WIN | DSSDPASQLSYSQEVGGPFKtPIKETLPISStPsKSVLPRt |
| Q08050 | T611 | GPS6|SIGNOR|iPTMNet|EPSD|PSP | FOXM1 FKHL16 HFH11 MPP2 WIN | SQEVGGPFKtPIKETLPISStPsKSVLPRtPEsWRLtPPAK |
| Q08050 | T620 | EPSD|PSP | FOXM1 FKHL16 HFH11 MPP2 WIN | tPIKETLPISStPsKSVLPRtPEsWRLtPPAKVGGLDFsPV |
| Q08379 | S37 | GPS6|SIGNOR|iPTMNet|EPSD | GOLGA2 | TRQSKLAAAKKKLREYQQRNsPGVPTGAKKKKKIKNGsNPE |
| Q08999 | S1044 | ELM | RBL2 RB2 | YSQANMDAPPLsPYPFVRtGsPRRIQLSQNHPVyIsPHKNE |
| Q08999 | S1068 | ELM | RBL2 RB2 | IQLSQNHPVyIsPHKNEtMLsPREKIFYYFsNsPsKRLREI |
| Q08999 | S1080 | ELM | RBL2 RB2 | PHKNEtMLsPREKIFYYFsNsPsKRLREINSMIRTGEtPTK |
| Q08999 | S1112 | ELM | RBL2 RB2 | IRTGEtPTKKRGILLEDGsEsPAKRICPENHSALLRRLQDV |
| Q08999 | S413 | ELM | RBL2 RB2 | KSKALRIStPLTGVRyIKENsPCVtPVSTATHSLSRLHTML |
| Q08999 | S662 | ELM | RBL2 RB2 | tPRRVtEVRADTGGLGRsItsPTtLyDRYssPPAStTRRRL |
| Q08999 | S688 | ELM | RBL2 RB2 | DRYssPPAStTRRRLFVENDsPsDGGtPGRMPPQPLVNAVP |
| Q08999 | T1097 | ELM | RBL2 RB2 | FsNsPsKRLREINSMIRTGEtPTKKRGILLEDGsEsPAKRI |
| Q08999 | T417 | ELM | RBL2 RB2 | LRIStPLTGVRyIKENsPCVtPVSTATHSLSRLHTMLTGLR |
| Q08999 | T642 | ELM | RBL2 RB2 | VMPPQNLERADEICIAGsPLtPRRVtEVRADTGGLGRsIts |
| Q08999 | T694 | ELM | RBL2 RB2 | PAStTRRRLFVENDsPsDGGtPGRMPPQPLVNAVPVQNVSG |
| Q08AD1 | S1319 | Sugiyama | CAMSAP2 CAMSAP1L1 KIAA1078 | NEsVHsGKRtPRsEsVEGFLsPsRCGsRNGEKDWENAstts |
| Q09472 | S1038 | SIGNOR|PSP | EP300 P300 | ELKTEIKEEEDQPstsAtQssPAPGQSKKKIFKPEELRQAL |
| Q09472 | S2039 | SIGNOR|PSP | EP300 P300 | AQHGQPLNMAPQPGLGQVGIsPLKPGTVSQQALQNLLRTLR |
| Q09666 | S41 | Sugiyama | AHNAK PM227 | HGLTIAQRDDGVFVQEVtQNsPAARTGVVKEGDQIVGATIy |
| Q09666 | S5763 | EPSD|PSP | AHNAK PM227 | LKssKAsLGsLEGEAEAEAssPKGKFSLFKSKKPRHRsNsF |
| Q12778 | S249 | GPS6|SIGNOR|EPSD|PSP | FOXO1 FKHR FOXO1A | EGTGKssWWMLNPEGGKSGKsPRRRAAsMDNNSKFAKSRSR |
| Q12792 | S143 | Sugiyama | TWF1 PTK9 | GTVKEDVSLHGYKKyLLsQssPAPLtAAEEELRQIKINEVQ |
| Q12802 | S2726 | Sugiyama | AKAP13 BRX HT31 LBC | EPPsPsAPSIAKsGsLDsELsVsPKRNsISRTHKDKGPFHI |
| Q12802 | S2728 | Sugiyama | AKAP13 BRX HT31 LBC | PsPsAPSIAKsGsLDsELsVsPKRNsISRTHKDKGPFHILS |
| Q12802 | T54 | GPS6 | AKAP13 BRX HT31 LBC | LVFLGSTLRHCTSTRKVSSDtLETIAPGHDCCETVKVQLCA |
| Q12879 | S1232 | ELM | GRIN2A NMDAR2A | THCRSCLSNMPTYSGHFTMRsPFKCDACLRMGNLyDIDEDQ |
| Q12888 | S1678 | SIGNOR|EPSD|PSP | TP53BP1 | RAsMGVLsGKRKLItsEEERsPAKRGRKSAtVKPGAVGAGE |
| Q12888 | T1609 | EPSD|PSP | TP53BP1 | SLEQGNRLREQYGLGPYEAVtPLtKAADIsLDNLVEGKRKR |
| Q12931 | S568 | Sugiyama | TRAP1 HSP75 HSPC5 | ISVETDIVVDHYKEEKFEDRsPAAECLSEKETEELMAWMRN |
| Q12959 | S158 | SIGNOR|EPSD|PSP | DLG1 | sEKNLsEIENVHGFVSHSHIsPIKPTEAVLPSPPTVPVIPV |
| Q12959 | S443 | SIGNOR|EPSD|PSP | DLG1 | SSQPVDNHVsPSSFLGQtPAsPARYSPVSKAVLGDDEITRE |
| Q13009 | S1466 | PSP | TIAM1 | RRRRLARNRFtIDSDAVSASsPEKESQQPPGGGDTDRWVEE |
| Q13033 | S229 | Sugiyama | STRN3 GS2NA SG2NA | SEPNGsVETKNLEQILNGGEsPKQKGQEIKRSSGDVLETFN |
| Q13042 | S112 | EPSD|PSP | CDC16 ANAPC6 | VLDMEEPINKRLFEKYLKDEsGFKDPSSDWEMSQSSIKSSI |
| Q13042 | S560 | SIGNOR|EPSD|PSP | CDC16 ANAPC6 | DKLKCYDFDVHTMKTLKNIIsPPWDFREFEVEKQTAEEtGL |
| Q13042 | T581 | EPSD|PSP | CDC16 ANAPC6 | PPWDFREFEVEKQTAEEtGLtPLEtsRKTPDSRPSLEETFE |
| Q13045 | S856 | Sugiyama | FLII FLIL | KNWDDVLTVDYTRNAEAVLQsPGLsGKVKRDAEKKDQMKAD |
| Q13049 | S328 | PSP | TRIM32 HT2A | AMEATASAASTSVTFREMDMsPEEVVAsPRAsPAKQRGPEA |
| Q13049 | S335 | PSP | TRIM32 HT2A | AASTSVTFREMDMsPEEVVAsPRAsPAKQRGPEAASNIQQC |
| Q13049 | S339 | PSP | TRIM32 HT2A | SVTFREMDMsPEEVVAsPRAsPAKQRGPEAASNIQQCLFLK |
| Q13153 | T212 | ELM | PAK1 | PRPEHTKsVytRsVIEPLPVtPtRDVAtsPIsPtENNttPP |
| Q13188 | S385 | EPSD|PSP | STK3 KRS1 MST2 | MVINSEDEEEEDGtMKRNAtsPQVQRPsFMDyFDKQDFKNK |
| Q13200 | S16 | Sugiyama | PSMD2 TRAP2 | _____MEEGGRDKAPVQPQQsPAAAPGGtDEKPsGKERRDA |
| Q13242 | S211 | Sugiyama | SRSF9 SFRS9 SRP30C | GYsRsRSGsRGRDsPyQsRGsPHyFsPFRPy__________ |
| Q13242 | S216 | Sugiyama | SRSF9 SFRS9 SRP30C | RSGsRGRDsPyQsRGsPHyFsPFRPy_______________ |
| Q13247 | S303 | Sugiyama | SRSF6 SFRS6 SRP55 | ENGKGDIKsKSRsRsQsRsNsPLPVPPsKARsVsPPPKRAT |
| Q13263 | S757 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | TLDLTLIRARLQEKLsPPyssPQEFAQDVGRMFKQFNKLTE |
| Q13283 | S231 | Sugiyama | G3BP1 G3BP | QEEKPEPVLEETAPEDAQKsssPAPADIAQtVQEDLRtFsW |
| Q13283 | S232 | Sugiyama | G3BP1 G3BP | EEKPEPVLEETAPEDAQKsssPAPADIAQtVQEDLRtFsWA |
| Q13409 | S97 | Sugiyama | DYNC1I2 DNCI2 DNCIC2 | FSEYWVPPPMsPSSKsVStPsEAGsQDsGDGAVGsRTLHWD |
| Q13415 | S258 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | ORC1 ORC1L PARC1 | ELGNLGNPQMSQQTSCAsLDsPGRIKRKVAFSEITsPsKRS |
| Q13415 | S273 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | ORC1 ORC1L PARC1 | CAsLDsPGRIKRKVAFSEITsPsKRSQPDKLQtLsPALKAP |
| Q13415 | T375 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | ORC1 ORC1L PARC1 | PENIKKRDAKEAKAQNEATstPHRIRRKSsVLTMNRIRQQL |
| Q13428 | S1378 | Sugiyama | TCOF1 | tPRSKKKKKLGAGEGGEAsVsPEKtsttSKGKAKRDKASGD |
| Q13428 | S156 | EPSD|PSP | TCOF1 | GNSMPHPATGKtVANLLsGKsPRKsAEPsANttLVsEtEEE |
| Q13428 | S583 | EPSD|PSP | TCOF1 | AVAPAQEKsLGNILQAKPtssPAKGPPQKAGPVAVQVKAEK |
| Q13428 | T983 | EPSD|PSP | TCOF1 | DPNRsPAGPAAtPAQAQAAstPRKARASESTARssssEsED |
| Q13501 | S272 | SIGNOR|EPSD|PSP | SQSTM1 ORCA OSIL | GIEVDIDVEHGGKRsRLtPVsPEssstEEKsssQPssCCsD |
| Q13501 | T269 | SIGNOR|EPSD|PSP | SQSTM1 ORCA OSIL | sPLGIEVDIDVEHGGKRsRLtPVsPEssstEEKsssQPssC |
| Q13509 | S115 | Sugiyama | TUBB3 TUBB4 | SGAGNNWAKGHytEGAELVDsVLDVVRKECENCDCLQGFQL |
| Q13509 | S172 | GPS6|EPSD | TUBB3 TUBB4 | ISKVREEYPDRIMNtFsVVPsPKVSDTVVEPYNATLSIHQL |
| Q13509 | S75 | Sugiyama | TUBB3 TUBB4 | SSHKYVPRAILVDLEPGtMDsVRSGAFGHLFRPDNFIFGQS |
| Q13535 | S428 | EPSD|PSP | ATR FRP1 | IEEIQCQTQQENLSSNSDGIsPKRRRLsSSLNPSKRAPKQT |
| Q13541 | S83 | EPSD|PSP | EIF4EBP1 | RNsPVtKtPPRDLPtIPGVtsPssDEPPMEAsQsHLRNsPE |
| Q13541 | T70 | SIGNOR|EPSD|PSP | EIF4EBP1 | tRIIyDRKFLMECRNsPVtKtPPRDLPtIPGVtsPssDEPP |
| Q13573 | S224 | Sugiyama | SNW1 SKIIP SKIP | KDPMEPPRFKINKKIPRGPPsPPAPVMHsPsRKMTVKEQQE |
| Q13573 | S234 | Sugiyama | SNW1 SKIIP SKIP | INKKIPRGPPsPPAPVMHsPsRKMTVKEQQEWKIPPCISNW |
| Q13586 | S668 | SIGNOR|EPSD|PSP | STIM1 GOK | AGKKAVAEEDNGsIGEEtDssPGRKKFPLKIFKKPLKK___ |
| Q13884 | S87 | Sugiyama | SNTB1 SNT2B1 | SFCRGAGAGHPGAGGAQPPDsPAGVRTAFTDLPEQVPESIS |
| Q13885 | S115 | Sugiyama | TUBB2A TUBB2 | sGAGNNWAKGHytEGAELVDsVLDVVRKESESCDCLQGFQL |
| Q13885 | S75 | Sugiyama | TUBB2A TUBB2 | AGNKYVPRAILVDLEPGtMDsVRsGPFGQIFRPDNFVFGQs |
| Q13950 | S451 | GPS6|EPSD | RUNX2 AML3 CBFA1 OSF2 PEBP2A | QSQSGPFQTSSTPYLYYGTSsGSYQFPMVPGGDRsPSRMLP |
| Q13950 | S465 | SIGNOR|EPSD|PSP | RUNX2 AML3 CBFA1 OSF2 PEBP2A | LYYGTSsGSYQFPMVPGGDRsPSRMLPPCTTTSNGSTLLNP |
| Q14005 | T757 | iPTMNet|EPSD|PSP | IL16 | PLQPNAsLNEEEGTQGHPDGtPPKLDTANGTPKVYKSADSS |
| Q14103 | S190 | Sugiyama | HNRNPD AUF1 HNRPD | KRAKAMKTKEPVKKIFVGGLsPDtPEEKIREYFGGFGEVES |
| Q14103 | T193 | Sugiyama | HNRNPD AUF1 HNRPD | KAMKTKEPVKKIFVGGLsPDtPEEKIREYFGGFGEVESIEL |
| Q14106 | S254 | SIGNOR|PSP | TOB2 KIAA1663 TOB4 TROB2 | SLSMHSLNFITANPAPQSQLsPNAKEFVYNGGGSPSLFFDA |
| Q14152 | S584 | Sugiyama | EIF3A EIF3S10 KIAA0139 | EHQRILARRQtIEERKERLEsLNIQREKEELEQREAELQKV |
| Q14157 | S416 | Sugiyama | UBAP2L KIAA0144 NICE4 | tQsPsLVQYDLKNPsDsAVHsPFtKRQAFtPsstMMEVFLQ |
| Q14157 | S454 | EPSD|PSP | UBAP2L KIAA0144 NICE4 | FLQEKsPAVAtstAAPPPPssPLPsKstsAPQMsPGssDNQ |
| Q14157 | S477 | Sugiyama | UBAP2L KIAA0144 NICE4 | PsKstsAPQMsPGssDNQsssPQPAQQKLKQQKKKAsLTSK |
| Q14157 | T419 | Sugiyama | UBAP2L KIAA0144 NICE4 | PsLVQYDLKNPsDsAVHsPFtKRQAFtPsstMMEVFLQEKs |
| Q14160 | S1232 | Sugiyama | SCRIB CRIB1 KIAA0147 LAP4 SCRB1 VARTUL | AAGIGHRNsLEsIssIDRELsPEGPGKEKELPGQTLHWGPE |
| Q14202 | T826 | EPSD|PSP | ZMYM3 DXS6673E KIAA0385 ZNF261 | PVKTRsAPtAPtPPPPPPPAtPRKNKAAMCKPLMQNRGVSC |
| Q14203 | S212 | EPSD|PSP | DCTN1 | AAPIIPTPVLTSPGAVPPLPsPSKEEEGLRAQVRDLEEKLE |
| Q14244 | S209 | EPSD|PSP | MAP7 | KyVDPVISKRLssssAtLLNsPDRARRLQLsPWESSVVNRL |
| Q14247 | S405 | EPSD|PSP|Sugiyama | CTTN EMS1 | EEARRKLEEQARAKtQtPPVsPAPQPtEERLPssPVyEDAA |
| Q14258 | S100 | Sugiyama | TRIM25 EFP RNF147 ZNF147 | DLAREPPADVWtPPARAsAPsPNAQVACDHCLKEAAVKTCL |
| Q14493 | T62 | GPS6|SIGNOR|EPSD|PSP | SLBP HBP | PEDAEEAEHRGAERRPEsFttPEGPKPRSRCSDWASAVEED |
| Q14568 | T109 | Sugiyama | HSP90AA2P HSP90AA2 HSPC2 HSPCAL3 | LTIVDTGIGMTKADLINNLGtIAKSGtKAFMEALQAGADIS |
| Q14643 | S421 | EPSD|PSP | ITPR1 INSP3R1 | STNIPIDKEEEKPVMLKIGTsPVKEDKEAFAIVPVsPAEVR |
| Q14643 | T800 | EPSD|PSP | ITPR1 INSP3R1 | ASFCRLMLHMHVDRDPQEQVtPVKYARLWSEIPSEIAIDDY |
| Q14674 | S1126 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | ESPL1 ESP1 KIAA0165 | LELVATVAKEPGPIAPstNssPVLKTKPQPIPNFLSHSPTC |
| Q14676 | T150 | Sugiyama | MDC1 KIAA0170 NFBD1 | YHRLDVSLPFVSRGPLTVEEtPRVQGEtQPQRLLLAEDsEE |
| Q14739 | S71 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | LBR | ENDIKPLtsFRQRKGGstsssPsRRRGSRSRSRsRsPGRPP |
| Q14739 | S86 | GPS6|EPSD | LBR | GstsssPsRRRGSRSRSRsRsPGRPPKsARRsAsAsHQADI |
| Q14790 | S387 | GPS6|SIGNOR|EPSD|PSP | CASP8 MCH5 | KGIPVETDSEEQPyLEMDLSsPQTRYIPDEADFLLGMATVN |
| Q14807 | S427 | EPSD|PSP | KIF22 KID KNSL4 | EEEIGsPEPMAAPAsAsQKLsPLQKLSSMDPAMLERLLsLD |
| Q14807 | T463 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | KIF22 KID KNSL4 | LLsLDRLLASQGsQGAPLLstPKRERMVLMKTVEEKDLEIE |
| Q14847 | T104 | Sugiyama | LASP1 MLN50 | VRYKEEFEKNKGKGFsVVADtPELQRIKKTQDQIsNIKyHE |
| Q14978 | T607 | EPSD|PSP | NOLC1 KIAA0035 NS5ATP13 | KQNEAAKEAEtPQAKKIKLQtPNtFPKRKKGEKRAssPFRR |
| Q14978 | T610 | EPSD|PSP | NOLC1 KIAA0035 NS5ATP13 | EAAKEAEtPQAKKIKLQtPNtFPKRKKGEKRAssPFRRVRE |
| Q14980 | S1757 | Sugiyama | NUMA1 NMP22 NUMA | ITSKLPRtQPDGtsVPGEPAsPIsQRLPPKVEsLEsLyFtP |
| Q14980 | S2087 | EPSD|PSP | NUMA1 NMP22 NUMA | GASKKALsKAsPNTRSGtRRsPRIATttAsAAtAAAIGAtP |
| Q14980 | T2000 | Sugiyama | NUMA1 NMP22 NUMA | GITTRQQRKRVsLEPHQGPGtPEsKKATSCFPRPMtPRDRH |
| Q14980 | T2015 | EPSD|PSP | NUMA1 NMP22 NUMA | HQGPGtPEsKKATSCFPRPMtPRDRHEGRKQSTTEAQKKAA |
| Q14980 | T2055 | SIGNOR|EPSD|PSP | NUMA1 NMP22 NUMA | APASTKQADRRQsMAFsILNtPKKLGNsLLRRGASKKALsK |
| Q14980 | T2106 | EPSD|PSP | NUMA1 NMP22 NUMA | RsPRIATttAsAAtAAAIGAtPRAKGKAKH___________ |
| Q14C86 | S466 | Sugiyama | GAPVD1 GAPEX5 KIAA1521 RAP6 | PAKPGKSSSLEMTPyNTPQLsPATTPANKKNRLPIATRSRS |
| Q14C86 | S950 | EPSD|PSP | GAPVD1 GAPEX5 KIAA1521 RAP6 | PPAAAIGATSLVAAPHSSSSsPSKDSSRGETEERKDSDDEK |
| Q14CB8 | T404 | EPSD|PSP | ARHGAP19 | PEsAKKKQLIRQFNKQSLTQtPGREPSTSQVQKRARsRsFS |
| Q14CB8 | T476 | EPSD|PSP | ARHGAP19 | KGTSKENRNLLFsGsPAVtMtPtRLKWSEGKKEGKKGFL__ |
| Q14CS0 | S56 | SIGNOR|EPSD|PSP | UBXN2B | EDEVKCKSSKSNRPKATVFKsPRtPPQRFYssEHEYSGLNI |
| Q14CS0 | T59 | SIGNOR|EPSD|PSP | UBXN2B | VKCKSSKSNRPKATVFKsPRtPPQRFYssEHEYSGLNIVRP |
| Q15003 | S81 | Sugiyama | NCAPH BRRN BRRN1 CAPH KIAA0074 | EKERLQRRRsRVFDLQFstDsPRLLAsPsSRsIDIsATIPK |
| Q15067 | S26 | Sugiyama | ACOX1 ACOX | RRERDSASFNPELLtHILDGsPEKtRRRREIENMILNDPDF |
| Q15116 | S261 | SIGNOR|PSP | PDCD1 PD1 | CVPEQTEyATIVFPSGMGTSsPARRGSADGPRSAQPLRPED |
| Q15149 | T4539 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | PLEC PLEC1 | EAGQRFLEVQYLTGGLIEPDtPGRVPLDEALQRGTVDARTA |
| Q15154 | S69 | Sugiyama | PCM1 | KKKFGVESDKRVTNDISPESsPGVGRRRTKTPHTFPHSRYM |
| Q15181 | S250 | Sugiyama | PPA1 IOPPP PP | LVTKKTNGKGIsCMNttLsEsPFKCDPDAARAIVDALPPPC |
| Q15233 | T15 | GPS6 | NONO NRB54 | ______MQSNKTFNLEKQNHtPRKHHQHHHQQQHHQQQQQQ |
| Q15233 | T410 | GPS6 | NONO NRB54 | GGAMGINNRGAMPPAPVPAGtPAPPGPAtMMPDGtLGLtPP |
| Q15233 | T428 | GPS6 | NONO NRB54 | AGtPAPPGPAtMMPDGtLGLtPPttERFGQAAtMEGIGAIG |
| Q15233 | T450 | GPS6 | NONO NRB54 | PttERFGQAAtMEGIGAIGGtPPAFNRAAPGAEFAPNKRRR |
| Q15291 | S497 | GPS6|EPSD | RBBP5 RBQ3 | GKSKKKQAGRPKGSKGKEKDsPFKPKLYKGDRGLPLEGsAK |
| Q15291 | T252 | GPS6|EPSD | RBBP5 RBQ3 | TCGRDGEPEPMQKLQDLVNRtPWKKCCFSGDGEYIVAGSAR |
| Q15293 | T76 | Sugiyama | RCN1 RCN | FQYDHEAFLGKEDsKtFDQLtPDEsKERLGKIVDRIDNDGD |
| Q15393 | T1200 | Sugiyama | SF3B3 KIAA0017 SAP130 | EQFNsMEPNKQKNVSEELDRtPPEVSKKLEDIRTRYAF___ |
| Q15398 | S618 | GPS6|EPSD|PSP | DLGAP5 DLG7 KIAA0008 | SVIPKEVDKIVFDAGFFRVEsPVKLFsGLsVssEGPsQRLG |
| Q15398 | S642 | GPS6|EPSD | DLGAP5 DLG7 KIAA0008 | LFsGLsVssEGPsQRLGtPKsVNKAVSQSRNEMGIPQQtts |
| Q15398 | S67 | GPS6|EPSD | DLGAP5 DLG7 KIAA0008 | LKDVNIPtLEGRILVELDETsQGLVPEKTNVKPRAMKTILG |
| Q15398 | S839 | GPS6|EPSD|PSP | DLGAP5 DLG7 KIAA0008 | ERRHQEHARHIsFGGNLItFsPLQPGEF_____________ |
| Q15398 | T329 | GPS6|EPSD|PSP | DLGAP5 DLG7 KIAA0008 | PKDFMFQPLDGLKTyQVTPMtPRsANAFLtPsytWtPLKTE |
| Q15398 | T401 | GPS6|EPSD | DLGAP5 DLG7 KIAA0008 | CPLGPLTVWHEEHVLNKNEAttKNLNGLPIKEVPsLERNEG |
| Q15398 | T402 | GPS6|EPSD | DLGAP5 DLG7 KIAA0008 | PLGPLTVWHEEHVLNKNEAttKNLNGLPIKEVPsLERNEGR |
| Q15398 | T639 | GPS6|EPSD|PSP | DLGAP5 DLG7 KIAA0008 | PVKLFsGLsVssEGPsQRLGtPKsVNKAVSQSRNEMGIPQQ |
| Q15398 | T759 | GPS6|EPSD | DLGAP5 DLG7 KIAA0008 | TNKKEGISDVVEGMELNSsItSQDVLMssPEKNTAsQNsIL |
| Q15637 | S80 | Sugiyama | SF1 ZFM1 ZNF162 | DLTRKLRtGDLGIPPNPEDRsPsPEPIyNsEGKRLNTREFR |
| Q15637 | S82 | Sugiyama | SF1 ZFM1 ZNF162 | TRKLRtGDLGIPPNPEDRsPsPEPIyNsEGKRLNTREFRTR |
| Q15642 | S299 | Sugiyama | TRIP10 CIP4 STOT STP | PGDVEFEDFsQPMNRAPsDssLGtPsDGRPELRGPGRSRTK |
| Q15717 | S202 | EPSD|PSP | ELAVL1 HUR | KFAANPNQNKNVALLsQLyHsPARRFGGPVHHQAQRFRFsP |
| Q15738 | S106 | Sugiyama | NSDHL H105E3 | CSRQDLyPALKGVNTVFHCAsPPPSSNNKELFYRVNYIGTK |
| Q15773 | S238 | Sugiyama | MLF2 | GAGGRRAEGPPRLAIQGPEDsPsRQsRRYDW__________ |
| Q15788 | T1426 | PSP | NCOA1 BHLHE74 SRC1 | DPYLNQPGPLGTQKPTSGPQtPQAQQKSLLQQLLTE_____ |
| Q15910 | T345 | GPS6|SIGNOR|EPSD|PSP | EZH2 KMT6 | YQHLEGAKEFAAALTAERIKtPPKRPGGRRRGRLPNNssRP |
| Q15910 | T487 | GPS6|SIGNOR|EPSD|PSP | EZH2 KMT6 | YEFRVKEssIIAPAPAEDVDtPPRKKKRKHRLWAAHCRKIQ |
| Q16204 | S244 | Sugiyama | CCDC6 D10S170 TST1 | LEAEKRILQEKLDQPVsAPPsPRDIsMEIDsPENMMRHIRF |
| Q16512 | S533 | SIGNOR|PSP | PKN1 PAK1 PKN PRK1 PRKCL1 | ATWVRLLRRLIPNAtGtGtFsPGAsPGsEARTTGDIsVEKL |
| Q16512 | S537 | SIGNOR|PSP | PKN1 PAK1 PKN PRK1 PRKCL1 | RLLRRLIPNAtGtGtFsPGAsPGsEARTTGDIsVEKLNLGt |
| Q16512 | S562 | SIGNOR|PSP | PKN1 PAK1 PKN PRK1 PRKCL1 | ARTTGDIsVEKLNLGtDsDssPQKssRDPPssPssLssPIQ |
| Q16512 | S916 | SIGNOR|PSP | PKN1 PAK1 PKN PRK1 PRKCL1 | SGRTDVsNFDEEFtGEAPtLsPPRDARPLTAAEQAAFLDFD |
| Q16513 | S535 | EPSD|PSP | PKN2 PRK2 PRKCL2 | ATWGRLVRRAIPtVNHsGtFsPQAPVPTTVPVVDVRIPQLA |
| Q16584 | S548 | SIGNOR|PSP | MAP3K11 MLK3 PTK1 SPRK | PRFRAIQLEPAEPGQAWGRQsPRRLEDssNGERRACWAWGP |
| Q16630 | T157 | Sugiyama | CPSF6 CFIM68 | SKKLMDLLPKRELHGQNPVVtPCNKQFLsQFEMQSRKTTQS |
| Q16659 | S684 | SIGNOR|EPSD|PSP | MAPK6 ERK3 PRKM6 | NsGEFLFNKQLEsIGIPQFHsPVGsPLKSIQATLtPSAMKs |
| Q16659 | S688 | SIGNOR|EPSD|PSP | MAPK6 ERK3 PRKM6 | FLFNKQLEsIGIPQFHsPVGsPLKSIQATLtPSAMKssPQI |
| Q16659 | S705 | SIGNOR|EPSD|PSP | MAPK6 ERK3 PRKM6 | PVGsPLKSIQATLtPSAMKssPQIPHQTYSSILKHLN____ |
| Q16659 | T698 | SIGNOR|EPSD|PSP | MAPK6 ERK3 PRKM6 | GIPQFHsPVGsPLKSIQATLtPSAMKssPQIPHQTYSSILK |
| Q16665 | S668 | EPSD|PSP | HIF1A BHLHE78 MOP1 PASD8 | HKETTSATSsPYRDTQSRTAsPNRAGKGVIEQTEKSHPRsP |
| Q16881 | T413 | Sugiyama | TXNRD1 GRIM12 KDRF | HGIKFIRQFVPIKVEQIEAGtPGRLRVVAQSTNSEEIIEGE |
| Q2M2I8 | T389 | EPSD|PSP | AAK1 KIAA1048 | RPKAGQTQPNPGILPIQPALtPRKRATVQPPPQAAGSSNQP |
| Q2NKX8 | T1063 | SIGNOR|EPSD|PSP | ERCC6L PICH | INPFNTSLFQFSsVKQFDAStPKNDIsPPGRFFssQIPssV |
| Q32P44 | T881 | PSP | EML3 | DASIFQWRVLGAGGAGPAPAtPsRtPsLsPAssLDV_____ |
| Q38SD2 | T1427 | EPSD|PSP | LRRK1 KIAA1790 | LSDYGISRQSFHEGALGVEGtPGYQAPEIRPRIVYDEKVDM |
| Q4KMP7 | T150 | Sugiyama | TBC1D10B FP2461 | ADsPKtEEARPsPAPGPGtPtGtPtRtPsRtAPGALTAKPP |
| Q53EL6 | S94 | Sugiyama | PDCD4 H731 | GDsVsDsGsDALRSGLtVPtsPKGRLLDRRSRSGKGRGLPK |
| Q53EZ4 | S425 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CEP55 C10orf3 URCC6 | ITEPLVTFQGETENREKVAAsPKsPtAALNEsLVECPKCNI |
| Q53EZ4 | S428 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CEP55 C10orf3 URCC6 | PLVTFQGETENREKVAAsPKsPtAALNEsLVECPKCNIQYP |
| Q53HL2 | S219 | PSP | CDCA8 PESCRG3 | tPGLRtPAAGERIyNIsGNGsPLADsKEIFLtVPVGGGEsL |
| Q58FF6 | T36 | Sugiyama | HSP90AB4P | LQELISNASDALDKIRyEsLtDPsKLDGGKELKIDIIPNPR |
| Q58FF7 | S370 | Sugiyama | HSP90AB3P HSP90BC | KETQKSTYYITGESKEQVANsAFVERVRKQGFEVVYMTEPI |
| Q58FF7 | S408 | Sugiyama | HSP90AB3P HSP90BC | EPIDEYCVQQLKEFDGKsLVsVtKEGLELPEDEEEKKKMEE |
| Q58FF7 | T60 | Sugiyama | HSP90AB3P HSP90BC | LQELISNASDALDKIRyEsLtDPsKLDsGKELKIDIIPNPQ |
| Q58FF8 | S308 | Sugiyama | HSP90AB2P HSP90BB | YMTEPIDGYQLKEFDGKsLVsVtKEGLELPEDGEEKKRMEE |
| Q58FF8 | T104 | Sugiyama | HSP90AB2P HSP90BB | LTLVDTGIGMTKADLINNLGtIAKFQDQTEYLEEMQVKEVV |
| Q58FF8 | T60 | Sugiyama | HSP90AB2P HSP90BB | LWELISNASDALDKIRyEsLtDPsKLDsGKELKIDIIPNTQ |
| Q5BJF6 | S820 | SIGNOR | ODF2 | LKSSYANVFGDGPystFLtssPIRsRsPPA___________ |
| Q5FBB7 | T346 | SIGNOR|EPSD|PSP | SGO1 SGOL1 | HKSVSSNDAYNFNLEEGVHLtPFRQKVSNDSNREENNESEV |
| Q5JSH3 | S96 | Sugiyama | WDR44 RPH11 | QLEDDsLDSKGKELsDQAtAsPIVARTDLSNIPGLLAIDQV |
| Q5SW79 | S1529 | Sugiyama | CEP170 FAM68A KAB KIAA0470 | PSAMLPsPPKQKssPVNNHHsPGQtPtLGQPEARALHPAAV |
| Q5T4S7 | S178 | Sugiyama | UBR4 KIAA0462 KIAA1307 RBAF600 | AKLPQTVKTLSDVEDQKELAsPVsPELRQKEVQMNFLNQLT |
| Q5T4S7 | S181 | Sugiyama | UBR4 KIAA0462 KIAA1307 RBAF600 | PQTVKTLSDVEDQKELAsPVsPELRQKEVQMNFLNQLTSVF |
| Q5T5Y3 | S563 | Sugiyama | CAMSAP1 | VAIVRADVVPQQADPEFPRAsPRALGLtANARsPQGQLDts |
| Q5TB30 | S110 | EPSD|PSP | DEPDC1 DEPDC1A | GRWGSENVDDNNQLFRFPATsPLKTLPRRYPELRKNNIENF |
| Q5UIP0 | S2161 | Sugiyama | RIF1 | NNAsPQKLRELDPsLVsANDsPsGMQtRCVWsPLAsPStsI |
| Q5UIP0 | S2163 | Sugiyama | RIF1 | AsPQKLRELDPsLVsANDsPsGMQtRCVWsPLAsPStsILK |
| Q5VT52 | S965 | Sugiyama | RPRD2 KIAA0460 HSPC099 | NsLsQsttGHLSLPQKQyPDsPHPVPHRsLFsPQNtLAAPT |
| Q68CZ2 | S660 | Sugiyama | TNS3 TEM6 TENS1 TPP | RVAVQRGVGsGPHPPDTQQPsPsKAFKPRFPGDQVVNGAGP |
| Q68CZ2 | S662 | Sugiyama | TNS3 TEM6 TENS1 TPP | AVQRGVGsGPHPPDTQQPsPsKAFKPRFPGDQVVNGAGPEL |
| Q69YH5 | T412 | PSP | CDCA2 | RVtFGEDLsPEVFDEsLPANtPLRKGGTPVCKKDFSGLSSL |
| Q69YN4 | S1579 | Sugiyama | VIRMA KIAA1429 MSTP054 | CCSDFDLHSELERsFLsEPssPGRtKTTKGFKLGKHKHETF |
| Q6P1L8 | S49 | Sugiyama | MRPL14 MRPL32 RPML32 | LSAIQKMTRVRVVDNSALGNsPyHRAPRCIHVYKKNGVGKV |
| Q6P1N0 | S208 | GPS6|SIGNOR|EPSD | CC2D1A AKI1 LGD2 | EADIPPPVAIGKGPAstPtysPAPTQPAPRIASAPEPRVTL |
| Q6PEY2 | T56 | Sugiyama | TUBA3E | MPSDKtIGGGDDsFNtFFsEtGAGKHVPRAVFVDLEPtVVD |
| Q6PGQ7 | S112 | EPSD|PSP | BORA C13orf34 | VEDKRQKAIEEFFTKDVIVPsPWTDHEGKQLSQCHSSKCTN |
| Q6PGQ7 | S137 | EPSD|PSP | BORA C13orf34 | HEGKQLSQCHSSKCTNINSDsPVGKKLTIHSEKSDAACQTL |
| Q6PGQ7 | S252 | EPSD|PSP | BORA C13orf34 | LSPVKCRsPLQTPSSGQFsssPIQASAKKYSLGSITsPsPI |
| Q6PGQ7 | S41 | EPSD|PSP | BORA C13orf34 | VLNPFESPSDYSNLHEQTLAsPSVFKSTKLPtPGKFRWSID |
| Q6PKG0 | S774 | Sugiyama | LARP1 KIAA0731 LARP | LFGAPEPstIARsLPttVPEsPNyRNtRtPRtPRtPQLKDS |
| Q6UN15 | S492 | Sugiyama | FIP1L1 FIP1 RHE | DRDRDRERERTRERERERDHsPtPsVFNsDEERyRYREYAE |
| Q6UVJ0 | S510 | PSP | SASS6 SAS6 | LGPSttPPAHSSSNTIRsGIsPNLNVVDGRLTYPTCGIGYP |
| Q6UVJ0 | T495 | PSP | SASS6 SAS6 | NKELNENQLVRKQDVLGPSttPPAHSSSNTIRsGIsPNLNV |
| Q6Y7W6 | S30 | EPSD|PSP | GIGYF2 KIAA0642 PERQ2 TNRC15 | FGPEWLRALssGGsItsPPLsPALPKYKLADYRYGREEMLA |
| Q6ZMR3 | S161 | Sugiyama | LDHAL6A LDHL2 | DILTYVAWKLSGFPKNRVIGsGCNLDsARFRYFIGQRLGIH |
| Q71U36 | T56 | Sugiyama | TUBA1A TUBA3 | MPSDKtIGGGDDsFNtFFsEtGAGKHVPRAVFVDLEPtVID |
| Q71U36 | T73 | Sugiyama | TUBA1A TUBA3 | FsEtGAGKHVPRAVFVDLEPtVIDEVRtGtyRQLFHPEQLI |
| Q71U36 | Y83 | Sugiyama | TUBA1A TUBA3 | PRAVFVDLEPtVIDEVRtGtyRQLFHPEQLItGKEDAANNy |
| Q7KZI7 | S456 | PSP | MARK2 EMK1 | RPEEDRESGRKAsstAKVPAsPLPGLERKKttPtPstNSVL |
| Q7KZI7 | S569 | PSP | MARK2 EMK1 | TEsNCEVPRPstAPQRVPVAsPsAHNIsssGGAPDRTNFPR |
| Q7KZI7 | S619 | PSP | MARK2 EMK1 | AGQLRQVRDQQNLPyGVtPAsPsGHsQGRRGAsGsIFSKFT |
| Q7L2J0 | S216 | Sugiyama | MEPCE BCDIN3 | NLNSLLDEEVSRtLNAEtPKssPLPAKGRDPVEILIPKDIt |
| Q7L2J0 | T208 | Sugiyama | MEPCE BCDIN3 | GGNIFDPLNLNSLLDEEVSRtLNAEtPKssPLPAKGRDPVE |
| Q7L2J0 | T213 | Sugiyama | MEPCE BCDIN3 | DPLNLNSLLDEEVSRtLNAEtPKssPLPAKGRDPVEILIPK |
| Q7Z3J3 | S1276 | EPSD|PSP | RGPD4 RGP4 | EDALDDsVssssVHAsPLAssPVRKNLFHFGESTTGSNFSF |
| Q7Z460 | T1099 | Sugiyama | CLASP1 KIAA0622 MAST1 | NHLKNssNtsVGsPsNtIGRtPsRHtssRTSPLTSPTNCSH |
| Q7Z4H7 | T858 | Sugiyama | HAUS6 DGT6 FAM29A KIAA1574 | EALKKSLSKKREESyLSNsQtPERHKPELsPtPQNVQtDDt |
| Q7Z5K2 | S221 | Sugiyama | WAPL FOE KIAA0261 WAPAL | AsEIKETNDTWNSQFGKRPEsPsEIsPIKGsVRTGLFEWDN |
| Q7Z5K2 | S226 | Sugiyama | WAPL FOE KIAA0261 WAPAL | ETNDTWNSQFGKRPEsPsEIsPIKGsVRTGLFEWDNDFEDI |
| Q7Z628 | S131 | GPS6 | NET1 ARHGEF8 | GAVRRFGQTIQSFTLRGDHRsPASAQKFSSRSTVPtPAKRR |
| Q7Z628 | T146 | GPS6 | NET1 ARHGEF8 | RGDHRsPASAQKFSSRSTVPtPAKRRSSALWSEMLDITMKE |
| Q86UE4 | S308 | Sugiyama | MTDH AEG1 LYRIC | EKSVKLssQIsAGEEKWNsVsPAsAGKRKtEPSAWsQDtGD |
| Q86UE4 | S568 | Sugiyama | MTDH AEG1 LYRIC | SNTKQNSVPPSQTKsEtsWEsPKQIKKKKKARRET______ |
| Q86UE4 | T143 | Sugiyama | MTDH AEG1 LYRIC | SEKPKPNGRTVEVAEGEAVRtPQsVtAKQPPEIDKKNEKSK |
| Q86VP6 | S376 | Sugiyama | CAND1 KIAA0829 TIP120 TIP120A | CLDAVVSTRHEMLPEFyKTVsPALISRFKEREENVKADVFH |
| Q86VV8 | S310 | Sugiyama | RTTN | SYCHEARGTHHSQNPsPGsssPRPSVVGRTGQRPRGDGQDW |
| Q86WB0 | S395 | SIGNOR|EPSD|PSP | ZC3HC1 NIPA HSPC216 | TRPVTRsMGtGDtPGLEVPssPLRKAKRARLCsssssDTSS |
| Q8IWB6 | T618 | SIGNOR|EPSD|PSP | TEX14 SGK307 | QNQDAPCPAPFMAEEASSPStGQPSLCSFEINEIYSGCLIL |
| Q8IWB6 | T727 | SIGNOR|EPSD|PSP | TEX14 SGK307 | SSLSLPESTREAKSNLNNMSttEEYLISKCVLDLKIMQTIM |
| Q8IWB6 | T728 | SIGNOR|EPSD|PSP | TEX14 SGK307 | SLSLPESTREAKSNLNNMSttEEYLISKCVLDLKIMQTIMH |
| Q8IX03 | S542 | EPSD|PSP | WWC1 KIAA0869 KIBRA | RsLSGtPKSMTSLsPRSsLSsPSPPCsPLMADPLLAGDAFL |
| Q8IX03 | S931 | EPSD|PSP | WWC1 KIAA0869 KIBRA | GtPsQGPFLRGSTIIRsKtFsPGPQSQYVCRLNRsDsDsST |
| Q8IX90 | S283 | PSP | SKA3 C13orf3 RAMA1 | FAtPsPIIQQLEKsDAEYtNsPLVPTFCtPGLKIPSTKNSI |
| Q8IX90 | T203 | PSP | SKA3 C13orf3 RAMA1 | KEEPVIVtPPTKQSLVKVLKtPKCALKMDDFECVtPKLEHF |
| Q8IX90 | T217 | PSP | SKA3 C13orf3 RAMA1 | LVKVLKtPKCALKMDDFECVtPKLEHFGISEYTMCLNEDYT |
| Q8IX90 | T291 | PSP | SKA3 C13orf3 RAMA1 | QQLEKsDAEYtNsPLVPTFCtPGLKIPSTKNSIALVSTNYP |
| Q8IX90 | T358 | EPSD|PSP | SKA3 C13orf3 RAMA1 | FENLtDPssPTISSYENLLRtPtPPEVTKIPEDILQLLSKY |
| Q8IX90 | T360 | EPSD|PSP | SKA3 C13orf3 RAMA1 | NLtDPssPTISSYENLLRtPtPPEVTKIPEDILQLLSKYNS |
| Q8IXJ6 | S368 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | SIRT2 SIR2L SIR2L2 | EHASIDAQSGAGVPNPstsAsPKKsPPPAKDEARTTEREKP |
| Q8IY92 | T1544 | PSP | SLX4 BTBD12 KIAA1784 KIAA1987 | TPPPAQMPSAGGAQKPEGLEtPKGANRKKNLPPKVPItPMP |
| Q8IY92 | T1561 | PSP | SLX4 BTBD12 KIAA1784 KIAA1987 | GLEtPKGANRKKNLPPKVPItPMPQYSIMEtPVLKKELDRF |
| Q8IY92 | T1571 | PSP | SLX4 BTBD12 KIAA1784 KIAA1987 | KKNLPPKVPItPMPQYSIMEtPVLKKELDRFGVRPLPKRQM |
| Q8IZD2 | T912 | EPSD|PSP | KMT2E MLL5 | PSPYATPTHTDITPMDPSFAtPPRIKSDDETCRNGYKPIYS |
| Q8IZP0 | S216 | GPS6|SIGNOR|EPSD|PSP | ABI1 SSH3BP1 | tPyKtLEPVKPPTVPNDyMtsPARLGsQHsPGRtAsLNQRP |
| Q8N122 | S696 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RPTOR KIAA1303 RAPTOR | SNFCTVALQFIEEEKNYALPsPATTEGGSLtPVRDsPCtPR |
| Q8N122 | T706 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RPTOR KIAA1303 RAPTOR | IEEEKNYALPsPATTEGGSLtPVRDsPCtPRLRsVssYGNI |
| Q8N556 | S264 | Sugiyama | AFAP1 AFAP | IKEAYSGCSGPVDSECPPPPssPVHKAELEKKLssERPssD |
| Q8N684 | T203 | Sugiyama | CPSF7 | GGIPPRAHsRDssDsADGRAtPsENLVPSSARVDKPPSVLP |
| Q8N884 | S305 | SIGNOR|PSP | CGAS C6orf150 MB21D1 | KEEINDIKDTDVIMKRKRGGsPAVTLLISEKISVDITLALE |
| Q8NBJ5 | S612 | Sugiyama | COLGALT1 GLT25D1 PSEC0241 | QKMREQQALSREAKNsDVLQsPLDsAARDEL__________ |
| Q8NBJ7 | S44 | Sugiyama | SUMF2 PSEC0171 UNQ1968/PRO4500 | NGQATSMVQLQGGRFLMGtNsPDSRDGDGPVREATVKPFAI |
| Q8NCD3 | S412 | PSP | HJURP FAKTS FLEG1 URLC9 | SSATYNLDEENRFRTLKWLIsPVKIVSRPTIRQGHGENRQR |
| Q8NCD3 | S448 | PSP | HJURP FAKTS FLEG1 URLC9 | ENRQREIEIRFDQLHREYCLsPRNQPRRMCLPDSWAMNMYR |
| Q8NCD3 | S473 | PSP | HJURP FAKTS FLEG1 URLC9 | PRRMCLPDSWAMNMYRGGPAsPGGLQGLETRRLsLPSSKAK |
| Q8NE01 | S700 | Sugiyama | CNNM3 ACDP3 | EKtttAAGssHsRPGVPVEGsPGRNPGV_____________ |
| Q8NEB9 | T159 | SIGNOR|EPSD|PSP | PIK3C3 VPS34 | GMHDLKVWPNVEADGSEPTKtPGRTsSTLSEDQMSRLAKLT |
| Q8NEL9 | S11 | PSP | DDHD1 KIAA1705 | __________MNyPGRGsPRsPEHNGRGGGGGAWELGSDAR |
| Q8NEL9 | S727 | PSP | DDHD1 KIAA1705 | KEPtsVSENEGIstIPsPVtsPVLsRRHYGESITNIGKASI |
| Q8NEL9 | S8 | PSP | DDHD1 KIAA1705 | _____________MNyPGRGsPRsPEHNGRGGGGGAWELGS |
| Q8NEN9 | S519 | Sugiyama | PDZD8 PDZK8 | EDLAsDVRAQNEFKDEAQsLsHsPKRVPtTLsIKPLGAIsP |
| Q8NEN9 | S989 | Sugiyama | PDZD8 PDZK8 | KHtPNtsDNEGsDtEVCGPNsPsKRGNSTGIKLVRKEGGLD |
| Q8NFD5 | S1744 | Sugiyama | ARID1B BAF250B DAN15 KIAA1235 OSA2 | ALDTINILLYDDSTVATFNLsQLSGFLELLVEYFRKCLIDI |
| Q8NFH8 | S463 | SIGNOR|EPSD|PSP | REPS2 POB1 | DPATPKDSNSLKARPRsRsYsstsIEEAMKRGEDPPtPPPR |
| Q8NFI4 | S181 | Sugiyama | ST13P5 FAM10A5 | LQKPNAAIQDCDRAIEINPDsAQPyKWRGKAHRLLGHWEEA |
| Q8NHV4 | S411 | PSP | NEDD1 | KNQDFssFDDtGKssLGDMFsPIRDDAVVNKGsDEsIGKGD |
| Q8NHV4 | S460 | SIGNOR|PSP | NEDD1 | NSVFPPRKNPVTsstsVLHssPLNVFMGsPGKEENENRDLT |
| Q8NHV4 | T550 | GPS6|SIGNOR|EPSD|PSP | NEDD1 | KPENEIEAQLICEPPINGsstPNPKIAssVtAGVAssLsEK |
| Q8TAP9 | S104 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | MPLKIP C7orf11 TTDN1 | GGYPGSYSRsPAGsQQQFGYsPGQQQtHPQGsPRTStPFGs |
| Q8TAP9 | S93 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | MPLKIP C7orf11 TTDN1 | FPGGRFGsPsPGGYPGSYSRsPAGsQQQFGYsPGQQQtHPQ |
| Q8TAP9 | T120 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | MPLKIP C7orf11 TTDN1 | QFGYsPGQQQtHPQGsPRTStPFGsGRVREKRMsNELENYF |
| Q8TC07 | S675 | Sugiyama | TBC1D15 | TSAFQSNALPTLSASGARNDsPtQIPVssDVCRLtPA____ |
| Q8TD19 | T210 | SIGNOR|PSP | NEK9 KIAA1995 NEK8 NERCC | IKLGDYGLAKKLNSEYSMAEtLVGtPYYMSPELCQGVKYNF |
| Q8TEM1 | S1881 | SIGNOR|iPTMNet | NUP210 KIAA0906 PSEC0245 | PtsPNALPPARKAsPPsGLWsPAYAsH______________ |
| Q8TEW0 | S728 | Sugiyama | PARD3 PAR3 PAR3A | DDRERRIsHsLysGIEGLDEsPsRNAALsRIMGESGKYQLS |
| Q8TEW0 | S730 | Sugiyama | PARD3 PAR3 PAR3A | RERRIsHsLysGIEGLDEsPsRNAALsRIMGESGKYQLSPT |
| Q8TF76 | T128 | SIGNOR|EPSD|PSP | HASPIN GSG2 | sLtVtPRRLGLRARPPQKCStPCGPLRLPPFPsRDsGRLsP |
| Q8WUF5 | S113 | SIGNOR|PSP | PPP1R13L IASPP NKIP1 PPP1R13BL RAI | ADtPFGRsEsAPtLHPysPLsPKGRPssPRtPLyLQPDAyG |
| Q8WUF5 | S84 | SIGNOR|PSP | PPP1R13L IASPP NKIP1 PPP1R13BL RAI | PsRPPRYssssIPEPFGsRGsPRKAATDGADtPFGRsEsAP |
| Q8WUX9 | S3 | PSP | CHMP7 | __________________MWsPEREAEAPAGGDPAGLLPPE |
| Q8WUX9 | S441 | PSP | CHMP7 | LEAELEKLsLsEGGLVPssKsPKRQLEPTLKPL________ |
| Q8WVD3 | T27 | SIGNOR | RNF138 NARF HSD-4 HSD4 | AATSYTEDDFYCPVCQEVLKtPVRTTACQHVFCRKCFLTAM |
| Q8WVM8 | S303 | Sugiyama | SCFD1 C14orf163 KIAA0917 STXBP1L2 FKSG23 | DVLDFHLNRVNLEEssGVENsPAGARPKRKNKKsYDLtPVD |
| Q8WVV9 | S75 | Sugiyama | HNRNPLL HNRPLL SRRF BLOCK24 | GGGRsFsQPEAGGsHHKVsVsPVVHVRGLCEsVVEADLVEA |
| Q8WWK9 | T623 | SIGNOR|EPSD|PSP | CKAP2 LB1 TMAP | VKKKVQFDGTNsAFKELKFLtPVRRsRRLQEKTSKLPDMLK |
| Q8WX93 | S641 | EPSD|PSP | PALLD KIAA0992 CGI-151 | GLINGKANSNKsLPtPAVLLsPtKEPPPLLAKPKLDPLKLQ |
| Q8WX93 | S766 | EPSD|PSP | PALLD KIAA0992 CGI-151 | AsGHGtPAssPssssLPsPMsPtPRQFGRAPVPPFAQPFGA |
| Q8WYP5 | S1214 | Sugiyama | AHCTF1 ELYS TMBS62 MSTP108 | FSEFTPQSILRstLRstPLAsPsPsPGRsPQRLKEtRIsFV |
| Q8WYP5 | S1218 | Sugiyama | AHCTF1 ELYS TMBS62 MSTP108 | TPQSILRstLRstPLAsPsPsPGRsPQRLKEtRIsFVEEDV |
| Q8WYP5 | S1222 | Sugiyama | AHCTF1 ELYS TMBS62 MSTP108 | ILRstLRstPLAsPsPsPGRsPQRLKEtRIsFVEEDVHPKW |
| Q92530 | S153 | Sugiyama | PSMF1 | RIVSGIITPIHEQWEKANVssPHREFPPAtAREVDPLRIPP |
| Q92574 | S584 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | TSC1 KIAA0243 TSC | ESPAGDRECQTSLETsIFTPsPCKIPPPTRVGFGsGQPPPY |
| Q92574 | T1047 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP|Sugiyama | TSC1 KIAA0243 TSC | RGSSGSRGGGGssssssELstPEKPPHQRAGPFSSRWETTM |
| Q92574 | T417 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | TSC1 KIAA0243 TSC | PAPLCHsDDyVHIsLPQAtVtPPRKEERMDSARPCLHRQHH |
| Q92785 | T176 | Sugiyama | DPF2 BAF45D REQ UBID4 | RILEPDDFLDDLDDEDyEEDtPKRRGKGKSKGKGVGSARKK |
| Q92879 | S178 | Sugiyama | CELF1 BRUNOL2 CUGBP CUGBP1 NAB50 | RAMAQTAIKAMHQAQtMEGCssPMVVKFADTQKDKEQKRMA |
| Q92879 | S179 | Sugiyama | CELF1 BRUNOL2 CUGBP CUGBP1 NAB50 | AMAQTAIKAMHQAQtMEGCssPMVVKFADTQKDKEQKRMAQ |
| Q92890 | S299 | Sugiyama | UFD1 UFD1L | KKVEEDEAGGRFVAFsGEGQsLRKKGRKP____________ |
| Q92934 | S91 | SIGNOR|EPSD|PSP | BAD BBC6 BCL2L8 | sRHssyPAGtEDDEGMGEEPsPFRGRsRsAPPNLWAAQRYG |
| Q92963 | S209 | PSP | RIT1 RIBB RIT ROC1 | AVLAMEKKSKPKNSVWKRLKsPFRKKKDSVT__________ |
| Q92973 | S339 | Sugiyama | TNPO1 KPNB2 MIP1 TRN | SDIDIILLKGDVEEDEtIPDsEQDIRPRFHRSRTVAQQHDE |
| Q92974 | S960 | SIGNOR|PSP|Sugiyama | ARHGEF2 KIAA0651 LFP40 | ssDPDtGsEEEGssRLsPPHsPRDFtRMQDIPEEtEsRDGE |
| Q92993 | S86 | SIGNOR|EPSD|PSP | KAT5 HTATIP TIP60 | KKIQFPKKEAKTPTKNGLPGsRPGsPEREVPASAQASGKTL |
| Q92993 | S90 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | KAT5 HTATIP TIP60 | FPKKEAKTPTKNGLPGsRPGsPEREVPASAQASGKTLPIPV |
| Q93008 | S2547 | SIGNOR|PSP | USP9X DFFRX FAM USP9 | NNPQRTGQRAQENYEGSEEVsPPQTKDQ_____________ |
| Q93045 | S73 | iPTMNet | STMN2 SCG10 SCGN10 | AFELILKPPsPISEAPRTLAsPKKKDLsLEEIQKKLEAAEE |
| Q969R2 | S762 | PSP | OSBP2 KIAA1664 ORP4 OSBPL4 | AHYVLSGSWDEQMECSKVMHssPssPsSDGKQKTVYQTLSA |
| Q969R2 | S763 | PSP | OSBP2 KIAA1664 ORP4 OSBPL4 | HYVLSGSWDEQMECSKVMHssPssPsSDGKQKTVYQTLSAK |
| Q969R2 | S766 | PSP | OSBP2 KIAA1664 ORP4 OSBPL4 | LSGSWDEQMECSKVMHssPssPsSDGKQKTVYQTLSAKLLW |
| Q969R2 | S768 | PSP | OSBP2 KIAA1664 ORP4 OSBPL4 | GSWDEQMECSKVMHssPssPsSDGKQKTVYQTLSAKLLWKK |
| Q96AC1 | S175 | SIGNOR|PSP | FERMT2 KIND2 MIG2 PLEKHC1 | LDDQsEDEALELEGPLItPGsGsIyssPGLysKTMTPTyDA |
| Q96AC1 | S177 | SIGNOR|PSP | FERMT2 KIND2 MIG2 PLEKHC1 | DQsEDEALELEGPLItPGsGsIyssPGLysKTMTPTyDAHD |
| Q96AC1 | S180 | SIGNOR|PSP | FERMT2 KIND2 MIG2 PLEKHC1 | EDEALELEGPLItPGsGsIyssPGLysKTMTPTyDAHDGSP |
| Q96AC1 | S181 | PSP | FERMT2 KIND2 MIG2 PLEKHC1 | DEALELEGPLItPGsGsIyssPGLysKTMTPTyDAHDGSPL |
| Q96AC1 | S186 | SIGNOR|PSP | FERMT2 KIND2 MIG2 PLEKHC1 | LEGPLItPGsGsIyssPGLysKTMTPTyDAHDGSPLsPTSA |
| Q96C19 | S74 | EPSD|PSP|Sugiyama | EFHD2 SWS1 | ELSAKLLRRADLNQGIGEPQsPsRRVFNPytEFKEFSRKQI |
| Q96C36 | S304 | EPSD|PSP | PYCR2 | KTLLDRVKLEsPTVSTLtPssPGKLLTRSLALGGKKD____ |
| Q96EB6 | S540 | SIGNOR|EPSD|PSP | SIRT1 SIR2L1 | ELAYLSELPPtPLHVsEDsssPERtsPPDssVIVTLLDQAA |
| Q96EB6 | T530 | EPSD|PSP | SIRT1 SIR2L1 | ITEKPPRTQKELAYLSELPPtPLHVsEDsssPERtsPPDss |
| Q96FF9 | S126 | SIGNOR|EPSD|PSP | CDCA5 | HsVPAtPtstPVPNPEAEsssKEGELDARDLEMsKKVRRsY |
| Q96FF9 | S139 | SIGNOR|EPSD|PSP | CDCA5 | NPEAEsssKEGELDARDLEMsKKVRRsYsRLEtLGsAstst |
| Q96FF9 | S164 | SIGNOR|EPSD|PSP | CDCA5 | RsYsRLEtLGsAststPGRRsCFGFEGLLGAEDLSGVsPVV |
| Q96FF9 | S181 | EPSD|PSP | CDCA5 | GRRsCFGFEGLLGAEDLSGVsPVVCSKLTEVPRVCAKPWAP |
| Q96FF9 | S209 | EPSD|PSP | CDCA5 | TEVPRVCAKPWAPDMTLPGIsPPPEKQKRKKKKMPEILKTE |
| Q96FF9 | S21 | EPSD|PSP | CDCA5 | MSGRRTRSGGAAQRSGPRAPsPtKPLRRsQRKsGsELPSIL |
| Q96FF9 | S33 | SIGNOR|EPSD|PSP | CDCA5 | QRSGPRAPsPtKPLRRsQRKsGsELPSILPEIWPKtPSAAA |
| Q96FF9 | S75 | EPSD|PSP | CDCA5 | RKPIVLKRIVAHAVEVPAVQsPRRsPRIsFFLEKENEPPGR |
| Q96FF9 | S79 | EPSD|PSP | CDCA5 | VLKRIVAHAVEVPAVQsPRRsPRIsFFLEKENEPPGRELTK |
| Q96FF9 | S83 | SIGNOR|EPSD|PSP | CDCA5 | IVAHAVEVPAVQsPRRsPRIsFFLEKENEPPGRELTKEDLF |
| Q96FF9 | T111 | EPSD|PSP | CDCA5 | EPPGRELTKEDLFKtHsVPAtPtstPVPNPEAEsssKEGEL |
| Q96FF9 | T115 | EPSD|PSP | CDCA5 | RELTKEDLFKtHsVPAtPtstPVPNPEAEsssKEGELDARD |
| Q96FF9 | T151 | SIGNOR|EPSD|PSP | CDCA5 | LDARDLEMsKKVRRsYsRLEtLGsAststPGRRsCFGFEGL |
| Q96FF9 | T159 | EPSD|PSP | CDCA5 | sKKVRRsYsRLEtLGsAststPGRRsCFGFEGLLGAEDLSG |
| Q96FF9 | T48 | EPSD|PSP | CDCA5 | RsQRKsGsELPSILPEIWPKtPSAAAVRKPIVLKRIVAHAV |
| Q96GM8 | S425 | Sugiyama | TOE1 | MGIKAARPEIADRATsEVPGsQAsPNPVPGDGLHRAGFDAF |
| Q96GN5 | T129 | Sugiyama | CDCA7L HR1 JPO2 R1 | DDGKAsLVsEEEEDEEEDKAtPRRSRSRRSSIGLRVAFQFP |
| Q96GX5 | S875 | PSP | MASTL GW GWL THC2 | DDETDTSYFEARNtAQHLtVsGFsL________________ |
| Q96GX5 | T194 | SIGNOR|PSP | MASTL GW GWL THC2 | DFGLSKVTLNRDINMMDILTtPSMAKPRQDYSRtPGQVLSL |
| Q96GX5 | T207 | SIGNOR | MASTL GW GWL THC2 | NMMDILTtPSMAKPRQDYSRtPGQVLSLISsLGFNtPIAEK |
| Q96IF1 | S119 | EPSD|PSP | AJUBA JUB | LPLPQSLPPDFRLEPtAPALsPRSSFASSSAsDAsKPssPR |
| Q96IF1 | S175 | EPSD|PSP | AJUBA JUB | sRPCsNRTSGISMGYDQRHGsPLPAGPCLFGPPLAGAPAGY |
| Q96JH7 | S768 | SIGNOR|EPSD|PSP | VCPIP1 KIAA1850 VCIP135 | PstIRDGPssAPAtPtKAPysPtTSKEKKIRITTNDGRQSM |
| Q96JH7 | T761 | SIGNOR|EPSD|PSP | VCPIP1 KIAA1850 VCIP135 | GQPRtVsPstIRDGPssAPAtPtKAPysPtTSKEKKIRITT |
| Q96KB5 | T9 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | PBK TOPK | ____________MEGISNFKtPsKLsEKKKsVLCstPtINI |
| Q96L14 | S238 | Sugiyama | CEP170P1 CEP170L KIAA0470L | PSAMLPsPPKQKssPVNNHHsPGQtPtLGQPEARALHPAAV |
| Q96MH2 | S76 | Sugiyama | HEXIM2 L3 | EDLAGAVGGLGWNsRsPRtQsPGGCsAEAVLARKKHRRRPS |
| Q96PY5 | S1016 | SIGNOR|PSP | FMNL2 FHOD2 KIAA1902 | QALMEKLLEQEALMEQQDPKsPsHKSKRQQQELIAELRRRQ |
| Q96Q89 | T1644 | GPS6|SIGNOR|EPSD|PSP | KIF20B KRMP1 MPHOSPH1 | EIQFtPLQPNKMAVKHPGCttPVTVKIPKARKRKsNEMEED |
| Q96QE3 | S653 | SIGNOR|PSP | ATAD5 C17orf41 Elg1 FRAG1 | LSEKHSLYTAELITVPFDsEsPIRMKFTRISTPKKSKKKSN |
| Q96QK1 | Y791 | Sugiyama | VPS35 MEM3 TCCCTA00141 | HNtLEHLRLRREsPEsEGPIyEGLIL_______________ |
| Q96R06 | S135 | EPSD|PSP | SPAG5 | sEEAVDPLGNyMVKtIVLVPsPLGQQQDMIFEARLDTMAET |
| Q96R06 | S249 | EPSD|PSP | SPAG5 | REDLVPSESNAFLPSSVLWLsPStALAADFRVNHVDPEEEI |
| Q96RL1 | S677 | EPSD|PSP | UIMC1 RAP80 RXRIP110 | EEAGCSREMQSsFTRRDLNEsPVKsFVsIsEATDCLVDFKK |
| Q96T23 | S1375 | EPSD|PSP | RSF1 HBXAP XAP8 | GKVGsPLDysLVDLPstNGQsPGKAIENLIGKPtEKsQtPK |
| Q96T88 | S639 | SIGNOR|EPSD|PSP | UHRF1 ICBP90 NP95 RNF106 | EREKENSKREEEEQQEGGFAsPRTGKGKWKRKSAGGGPSRA |
| Q99459 | T396 | Sugiyama | CDC5L KIAA0432 PCDC5RP | DtPLKGGLNtPLHEsDFsGVtPQRQVVQtPNtVLstPFRtP |
| Q99638 | S277 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RAD9A | DGHFVLAtLsDtDsHsQDLGsPERHQPVPQLQAHStPHPDD |
| Q99638 | S328 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RAD9A | IAMETTIGNEGSRVLPsIsLsPGPQPPKsPGPHsEEEDEAE |
| Q99638 | S336 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RAD9A | NEGSRVLPsIsLsPGPQPPKsPGPHsEEEDEAEPStVPGtP |
| Q99638 | T292 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RAD9A | sQDLGsPERHQPVPQLQAHStPHPDDFANDDIDSYMIAMET |
| Q99638 | T355 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | RAD9A | KsPGPHsEEEDEAEPStVPGtPPPKKFRsLFFGsILAPVRs |
| Q99661 | T537 | SIGNOR|EPSD|PSP | KIF2C KNSL6 | NKsLLALKECIRALGQNKAHtPFRESKLTQVLRDSFIGENS |
| Q99666 | S1275 | EPSD|PSP | RGPD5 RANBP2L1 RGP5 RGP7 RGPD7; RGPD6 RANBP2L2 RGP6 | EDALDDsVssssVHAsPLAssPVRKNLFRFDESTTGSNFsF |
| Q99708 | S327 | PSP | RBBP8 CTIP | RFSDstsKtPPQEELPtRVssPVFGATSSIKSGLDLNTsLs |
| Q99708 | T847 | GPS6|EPSD | RBBP8 CTIP | EREKKLASCSRHRFRYIPPNtPENFWEVGFPStQTCMERGY |
| Q99728 | S148 | EPSD|PSP | BARD1 | PRKSLFNDAGNKKNSIKMWFsPRSKKVRYVVSKASVQTQPA |
| Q99728 | S251 | EPSD|PSP | BARD1 | SKEESKQKLVSFCSQPSVISsPQINGEIDLLASGSLTESEC |
| Q99728 | S288 | EPSD|PSP | BARD1 | ESECFGSLTEVSLPLAEQIEsPDTKSRNEVVtPEKVCKNYL |
| Q99728 | T299 | EPSD|PSP | BARD1 | SLPLAEQIEsPDTKSRNEVVtPEKVCKNYLTSKKSLPLENN |
| Q99733 | T51 | Sugiyama | NAP1L4 NAP2 | VMQNPRVLAALQERLDNVPHtPssyIEtLPKAVKRRINALK |
| Q99733 | T58 | Sugiyama | NAP1L4 NAP2 | LAALQERLDNVPHtPssyIEtLPKAVKRRINALKQLQVRCA |
| Q99733 | Y55 | Sugiyama | NAP1L4 NAP2 | PRVLAALQERLDNVPHtPssyIEtLPKAVKRRINALKQLQV |
| Q9BPX3 | T308 | EPSD|PSP | NCAPG CAPG NYMEL3 | LDVENSSEVAVSVLNALFSItPLSELVGLCKNNDGRKLIPV |
| Q9BPX3 | T332 | EPSD|PSP | NCAPG CAPG NYMEL3 | ELVGLCKNNDGRKLIPVETLtPEIALYWCALCEYLKSKGDE |
| Q9BPX3 | T931 | EPSD|PSP | NCAPG CAPG NYMEL3 | ATLTTTTFQNEDEKNKEVyMtPLRGVKATQASKSTQLKTNR |
| Q9BQ39 | T266 | Sugiyama | DDX50 | GTSYQSQINHIRNGIDILVGtPGRIKDHLQSGRLDLSKLRH |
| Q9BQ52 | S199 | Sugiyama | ELAC2 HPC2 | TVyQIPIHSEQRRGKHQPWQsPERPLsRLsPERssDsEsNE |
| Q9BQE3 | T56 | Sugiyama | TUBA1C TUBA6 | MPSDKtIGGGDDsFNtFFsEtGAGKHVPRAVFVDLEPtVID |
| Q9BQE3 | T73 | Sugiyama | TUBA1C TUBA6 | FsEtGAGKHVPRAVFVDLEPtVIDEVRtGtyRQLFHPEQLI |
| Q9BQE3 | Y83 | Sugiyama | TUBA1C TUBA6 | PRAVFVDLEPtVIDEVRtGtyRQLFHPEQLItGKEDAANNy |
| Q9BQG0 | S1163 | Sugiyama | MYBBP1A P160 | GVQRPKLEKKDAKEIPsAtQsPIsKKRKKKGFLPETKKRKK |
| Q9BQG0 | T1161 | Sugiyama | MYBBP1A P160 | TLGVQRPKLEKKDAKEIPsAtQsPIsKKRKKKGFLPETKKR |
| Q9BQL6 | S174 | SIGNOR|PSP | FERMT1 C20orf42 KIND1 URP1 | KNNKEPIIEDILNLEssPtAsGssVsPGLySKTMTPIYDPI |
| Q9BQL6 | S176 | SIGNOR|PSP | FERMT1 C20orf42 KIND1 URP1 | NKEPIIEDILNLEssPtAsGssVsPGLySKTMTPIYDPING |
| Q9BQL6 | S179 | SIGNOR|PSP | FERMT1 C20orf42 KIND1 URP1 | PIIEDILNLEssPtAsGssVsPGLySKTMTPIYDPINGTPA |
| Q9BQQ3 | S274 | SIGNOR | GORASP1 GOLPH5 GRASP65 | MEALLQAPGSSMEDPLPGPGsPSHSAPDPDGLPHFMETPLQ |
| Q9BQQ3 | S373 | SIGNOR | GORASP1 GOLPH5 GRASP65 | HERGGEATWSGSEFEVSFLDsPGAQAQADHLPQLTLPDSLT |
| Q9BRP1 | S20 | Sugiyama | PDCD2L | _MAAVLKPVLLGLRDAPVHGsPTGPGAWTASKLGGIPDALP |
| Q9BTA9 | T244 | SIGNOR|PSP | WAC KIAA1844 | tsRHNDRDYRLPRAETHsSstPVQHPIKPVVHPtAtPstVP |
| Q9BTA9 | T457 | SIGNOR|PSP | WAC KIAA1844 | PMsLTsDAssPRSYVSPRIstPQtNTVPIKPLIstPPVSSQ |
| Q9BTA9 | T471 | SIGNOR|PSP | WAC KIAA1844 | VSPRIstPQtNTVPIKPLIstPPVSSQPKVStPVVKQGPVs |
| Q9BTA9 | T482 | SIGNOR|PSP | WAC KIAA1844 | TVPIKPLIstPPVSSQPKVStPVVKQGPVsQSATQQPVtAD |
| Q9BUJ2 | S512 | Sugiyama | HNRNPUL1 E1BAP5 HNRPUL1 | IQIAARKKRNyILDQtNVyGsAQRRKMRPFEGFQRKAIVIC |
| Q9BVA1 | S115 | Sugiyama | TUBB2B | sGAGNNWAKGHytEGAELVDsVLDVVRKESESCDCLQGFQL |
| Q9BVA1 | S75 | Sugiyama | TUBB2B | tGNKYVPRAILVDLEPGtMDsVRsGPFGQIFRPDNFVFGQs |
| Q9BW19 | S26 | PSP | KIFC1 HSET KNSL2 | sPLLEVKGNIELKRPLIKAPsQLPLsGsRLKRRPDQMEDGL |
| Q9BW19 | S31 | PSP | KIFC1 HSET KNSL2 | VKGNIELKRPLIKAPsQLPLsGsRLKRRPDQMEDGLEPEKK |
| Q9BW19 | S6 | SIGNOR|PSP | KIFC1 HSET KNSL2 | _______________MDPQRsPLLEVKGNIELKRPLIKAPs |
| Q9BX68 | T47 | Sugiyama | HINT2 | QVRGAAGVTDGNEVAKAQQAtPGGAAPtIFsRILDKsLPAD |
| Q9BXB4 | S181 | Sugiyama | OSBPL11 ORP11 OSBP12 | IGKNNPPLKsRsFsLAsssNsPIsQRRPsQNAIsFFNVGHS |
| Q9BXR0 | S139 | Sugiyama | QTRT1 TGT TGUT | EVTEEGVRFRSPYDGNETLLsPEKSVQIQNALGSDIIMQLD |
| Q9BXS6 | T300 | SIGNOR|EPSD|PSP | NUSAP1 ANKT BM-037 PRO0310 | TGVRFsAATKDNEHKRSLTKtPARKsAHVTVsGGtPKGEAV |
| Q9BXS6 | T338 | SIGNOR|EPSD|PSP | NUSAP1 ANKT BM-037 PRO0310 | EAVLGTHKLKTITGNsAAVItPFKLTtEAtQtPVsNKKPVF |
| Q9BYG3 | T238 | SIGNOR|EPSD|PSP | NIFK MKI67IP NOPP34 | sGtLDtPEKtVDsQGPtPVCtPtFLERRKsQVAELNDDDKD |
| Q9C086 | S63 | Sugiyama | INO80B HMGA1L4 PAPA1 ZNHIT4 | HKKKHKKKHHQEEDAGPtQPsPAKPQLKLKIKLGGQVLGTK |
| Q9C0C2 | S1103 | Sugiyama | TNKS1BP1 KIAA1741 TAB182 | KRGWVGEFSLSVGPQREAAFsPGQQDWsRDFCIEASERsyQ |
| Q9C0C2 | S435 | Sugiyama | TNKS1BP1 KIAA1741 TAB182 | DAHLRPtsLVQRRFsEGVLQsPsQDQEKLGGsLAALPQGQG |
| Q9C0C2 | S437 | Sugiyama | TNKS1BP1 KIAA1741 TAB182 | HLRPtsLVQRRFsEGVLQsPsQDQEKLGGsLAALPQGQGsQ |
| Q9C0C2 | S672 | Sugiyama | TNKS1BP1 KIAA1741 TAB182 | TLARAETtQARtEAQDLCRAsPEPPGPEsSSRWLDDLLAsP |
| Q9C0C7 | S1252 | SIGNOR | AMBRA1 DCAF3 KIAA1736 | SWDQPGtPGREPTQPTLPSSsPVPIPVSLPSAEGPTLHCEL |
| Q9C0C7 | T1238 | SIGNOR | AMBRA1 DCAF3 KIAA1736 | AGQLAERGLsPRTASWDQPGtPGREPTQPTLPSSsPVPIPV |
| Q9GZM8 | S242 | GPS6|SIGNOR|EPSD|PSP | NDEL1 EOPA MITAP1 NUDEL | GKGTENTFPsPKAIPNGFGTsPLtPSARIsALNIVGDLLRK |
| Q9GZM8 | T219 | GPS6|SIGNOR|EPSD|PSP | NDEL1 EOPA MITAP1 NUDEL | PTLDCEKMDSAVQAsLsLPAtPVGKGTENTFPsPKAIPNGF |
| Q9GZM8 | T245 | GPS6|SIGNOR|EPSD|PSP | NDEL1 EOPA MITAP1 NUDEL | TENTFPsPKAIPNGFGTsPLtPSARIsALNIVGDLLRKVGA |
| Q9GZR2 | S15 | Sugiyama | REXO4 PMC2 XPMC2H | ______MGKAKVPASKRAPssPVAKPGPVKTLTRKKNKKKK |
| Q9GZV5 | S105 | SIGNOR|EPSD|PSP | WWTR1 TAZ | VRsHssPAsLQLGtGAGAAGsPAQQHAHLRQQsYDVTDELP |
| Q9GZV5 | S90 | SIGNOR|EPSD|PSP | WWTR1 TAZ | sGGHPGPRLAGGAQHVRsHssPAsLQLGtGAGAAGsPAQQH |
| Q9GZV5 | T285 | SIGNOR|EPSD|PSP | WWTR1 TAZ | LPMEAETLAPVQAAVNPPTMtPDMRSItNNssDPFLNGGPy |
| Q9GZV5 | T326 | SIGNOR|EPSD|PSP | WWTR1 TAZ | HsREQsTDsGLGLGCySVPTtPEDFLSNVDEMDTGENAGQt |
| Q9GZV5 | T346 | SIGNOR|EPSD|PSP | WWTR1 TAZ | tPEDFLSNVDEMDTGENAGQtPMNINPQQTRFPDFLDCLPG |
| Q9H0H5 | T588 | iPTMNet | RACGAP1 KIAA1478 MGCRACGAP | PDIKVSLLGPVttPEHQLLKtPssssLsQRVRstLTKNtPR |
| Q9H1A4 | S355 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | ANAPC1 TSG24 | PsLHsRsPsISNMAALsRAHsPALGVHsFsGVQRFNIssHN |
| Q9H1A4 | S373 | EPSD|PSP | ANAPC1 TSG24 | AHsPALGVHsFsGVQRFNIssHNQsPKRHSISHSPNSNSNG |
| Q9H1A4 | S377 | GPS6|ELM|iPTMNet|EPSD|PSP | ANAPC1 TSG24 | ALGVHsFsGVQRFNIssHNQsPKRHSISHSPNSNSNGSFLA |
| Q9H1A4 | S547 | EPSD|PSP | ANAPC1 TSG24 | RPstPLDGVstPKPLSKLLGsLDEVVLLsPVPELRDssKLH |
| Q9H1A4 | S555 | GPS6|ELM|iPTMNet|EPSD|PSP | ANAPC1 TSG24 | VstPKPLSKLLGsLDEVVLLsPVPELRDssKLHDsLYNEDC |
| Q9H1A4 | S688 | GPS6|ELM|iPTMNet|EPSD|PSP | ANAPC1 TSG24 | MGYNTDRLAWTRNFDFEGsLsPVIAPKKARPsEtGsDDDWE |
| Q9H1A4 | T291 | GPS6|ELM|iPTMNet|EPSD|PSP | ANAPC1 TSG24 | LRRVKSEEENVVLKFsEQGGtPQNVAtsssLTAHLRsLsKG |
| Q9H1A4 | T530 | GPS6|ELM|iPTMNet|EPSD|PSP | ANAPC1 TSG24 | FIPGLPAPsLtMsNtMPRPstPLDGVstPKPLSKLLGsLDE |
| Q9H1A4 | T537 | GPS6|ELM|iPTMNet|EPSD|PSP | ANAPC1 TSG24 | PsLtMsNtMPRPstPLDGVstPKPLSKLLGsLDEVVLLsPV |
| Q9H1A4 | T701 | EPSD|PSP | ANAPC1 TSG24 | FDFEGsLsPVIAPKKARPsEtGsDDDWEYLLNSDYHQNVES |
| Q9H1E3 | S181 | SIGNOR|EPSD|PSP | NUCKS1 NUCKS JC7 | KPERKEKKMPKPRLKAtVtPsPVKGKGKVGRPTAsKAsKEK |
| Q9H1E3 | S214 | Sugiyama | NUCKS1 NUCKS JC7 | AsKAsKEKtPsPKEEDEEPEsPPEKKtstsPPPEKsGDEGs |
| Q9H211 | S411 | PSP | CDT1 | sPGsPRPALPAtPPAtPPAAsPSALKGVSQDLLERIRAKEA |
| Q9H211 | T402 | PSP | CDT1 | LALRsAAPssPGsPRPALPAtPPAtPPAAsPSALKGVSQDL |
| Q9H211 | T406 | PSP | CDT1 | sAAPssPGsPRPALPAtPPAtPPAAsPSALKGVSQDLLERI |
| Q9H2U2 | S316 | Sugiyama | PPA2 HSPC124 | SDSPFRCtQEEARsLVEsVsssPNKEsNEEEQVWHFLGK__ |
| Q9H2U2 | S317 | Sugiyama | PPA2 HSPC124 | DSPFRCtQEEARsLVEsVsssPNKEsNEEEQVWHFLGK___ |
| Q9H410 | S331 | PSP | DSN1 C20orf172 MIS13 | QCFQKVSVQLGKRSMQQLDPsPARKLLKLQLQNPPAIHGsG |
| Q9H467 | S110 | GPS6|EPSD|PSP | CUEDC2 C10orf66 HOYS6 | ARNKENLQPQSSGVQGQVPIsPEPLQRPEMLKEETRSSAAA |
| Q9H4A3 | S1261 | Sugiyama | WNK1 HSN2 KDP KIAA0344 PRKWNK1 | GIPTSSLTQVVHSAGRRFIVsPVPEsRLRESKVFPSEITDT |
| Q9H4A3 | S2032 | Sugiyama | WNK1 HSN2 KDP KIAA0344 PRKWNK1 | sDPEAAFLSRDVDDGsGsPHsPHQLssKSLPSQNLSQSLSN |
| Q9H4X1 | T111 | GPS6|SIGNOR|iPTMNet|EPSD|PSP | RGCC C13orf15 RGC32 | sDEKLNsPtDstPALLsAtVtPQKAKLGDTKELEAFIADLD |
| Q9H6F5 | S102 | Sugiyama | CCDC86 CYCLON | QGQPEPGAAsPQRQQDLHLEsPQRQPEysPEsPRCQPKPSE |
| Q9H6F5 | S91 | Sugiyama | CCDC86 CYCLON | RLQQGAGLEsPQGQPEPGAAsPQRQQDLHLEsPQRQPEysP |
| Q9H773 | S85 | Sugiyama | DCTPP1 XTP3TPA CDA03 | GELAELFQWKTDGEPGPQGWsPRERAALQEELSDVLIYLVA |
| Q9H8V3 | T373 | GPS6|SIGNOR|EPSD|PSP | ECT2 | LYEKANtPELKKsVsMLsLNtPNsNRKRRRLKETLAQLsRE |
| Q9H8V3 | T444 | GPS6|SIGNOR|EPSD|PSP | ECT2 | ESSINYGDtPKSCTKSSKSStPVPSKQSARWQVAKELYQTE |
| Q9H8V3 | T846 | GPS6|SIGNOR|EPSD|PSP | ECT2 | ASRAIKKTSKKVTRAFsFSKtPKRALRRALMtsHGsVEGRs |
| Q9H9S0 | S65 | PSP | NANOG | MPHTETVsPLPSSMDLLIQDsPDsSTsPKGKQPtsAEKSVA |
| Q9H9S0 | S71 | PSP | NANOG | VsPLPSSMDLLIQDsPDsSTsPKGKQPtsAEKSVAKKEDKV |
| Q9HC35 | S146 | Sugiyama | EML4 C2orf2 EMAPL4 | REKKEEsHsNDQsPQIRAsPsPQPssQPLQIHRQtPEsKNA |
| Q9HCH0 | S440 | PSP | NCKAP5L CEP169 KIAA1602 FP1193 | RPGHPHSSSQVKSKLQIGPPsPGEAQGPLLPsPARGLKFLK |
| Q9HCH0 | S451 | PSP | NCKAP5L CEP169 KIAA1602 FP1193 | KSKLQIGPPsPGEAQGPLLPsPARGLKFLKLPPTSEKSPsP |
| Q9HCH0 | S470 | PSP | NCKAP5L CEP169 KIAA1602 FP1193 | PsPARGLKFLKLPPTSEKSPsPGGPQLsPQLPRNSRIPCRN |
| Q9HCH0 | S477 | PSP | NCKAP5L CEP169 KIAA1602 FP1193 | KFLKLPPTSEKSPsPGGPQLsPQLPRNSRIPCRNSGSDGSP |
| Q9HCH0 | S571 | PSP | NCKAP5L CEP169 KIAA1602 FP1193 | VVSPCYENILDLSRSTFRGPsPEPPPsPLQVPTYPQLTLEV |
| Q9HCH0 | S577 | PSP | NCKAP5L CEP169 KIAA1602 FP1193 | ENILDLSRSTFRGPsPEPPPsPLQVPTYPQLTLEVPQAPEV |
| Q9HCH0 | S767 | PSP | NCKAP5L CEP169 KIAA1602 FP1193 | PGARVYSSHSMGARVDLEPVsPRSCLTKVELAKSRLAGALC |
| Q9NQR1 | S100 | SIGNOR|EPSD|PSP | KMT5A PRSET7 SET07 SET8 SETD8 | RPRTDGENVFTGQSKIySYMsPNKCSGMRFPLQEENSVtHH |
| Q9NQR4 | S133 | Sugiyama | NIT2 CUA002 | IHLFDIDVPGKITFQESKTLsPGDsFSTFDTPyCRVGLGIC |
| Q9NQS7 | T412 | SIGNOR | INCENP | VPENNGNNsWPHNDtEIANstPNPKPAAssPEtPSAGQQEA |
| Q9NQS7 | T59 | PSP | INCENP | EEAERMFTREFSKEPELMPKtPSQKNRRKKRRIsYVQDENR |
| Q9NQX3 | S270 | Sugiyama | GPHN GPH KIAA1385 | SRGVQVLPRDTAsLsttPsEsPRAQAtsRLstAsCPtPKVQ |
| Q9NR30 | S71 | Sugiyama | DDX21 | VFPKAKQVKKKAEPSEVDMNsPKSKKAKKKEEPSQNDIsPK |
| Q9NR30 | T315 | Sugiyama | DDX21 | GtPYGGQFERMRNGIDILVGtPGRIKDHIQNGKLDLTKLKH |
| Q9NRI5 | S713 | PSP | DISC1 KIAA0457 | ADLEACRLLIQSLQLQEARGsLSVEDERQMDDLEGAAPPIP |
| Q9NTG7 | S159 | SIGNOR|EPSD|PSP | SIRT3 SIR2L3 | RVVVMVGAGIStPSGIPDFRsPGSGLYSNLQQYDLPYPEAI |
| Q9NTG7 | T150 | SIGNOR|EPSD|PSP | SIRT3 SIR2L3 | ELIRARACQRVVVMVGAGIStPSGIPDFRsPGSGLYSNLQQ |
| Q9NTI5 | S1283 | Sugiyama | PDS5B APRIN AS3 KIAA0979 | QWPEEKRLKEDILENEDEQNsPPKKGKRGRPPKPLGGGtPK |
| Q9NTI5 | T1370 | EPSD|PSP | PDS5B APRIN AS3 KIAA0979 | RRAQQRAEsPEssAIEstQstPQKGRGRPsKtPsPsQPKKN |
| Q9NXR1 | S239 | iPTMNet | NDE1 NUDE | HRGPsssLNtPGsFRRGLDDstGGtPLtPAARISALNIVGD |
| Q9NXR1 | S282 | SIGNOR|PSP | NDE1 NUDE | RKVGALESKLASCRNLVyDQsPNRTGGPASGRSSKNRDGGE |
| Q9NXR1 | T191 | SIGNOR|PSP | NDE1 NUDE | DEARDLRQELAVQQKQEKPRtPMPSsVEAERTDTAVQAtGs |
| Q9NXR1 | T215 | SIGNOR|iPTMNet|PSP | NDE1 NUDE | SsVEAERTDTAVQAtGsVPstPIAHRGPsssLNtPGsFRRG |
| Q9NXR1 | T228 | SIGNOR|PSP | NDE1 NUDE | AtGsVPstPIAHRGPsssLNtPGsFRRGLDDstGGtPLtPA |
| Q9NXR1 | T243 | SIGNOR|PSP | NDE1 NUDE | sssLNtPGsFRRGLDDstGGtPLtPAARISALNIVGDLLRK |
| Q9NXR1 | T246 | SIGNOR|EPSD|PSP | NDE1 NUDE | LNtPGsFRRGLDDstGGtPLtPAARISALNIVGDLLRKVGA |
| Q9NY27 | S224 | Sugiyama | PPP4R2 SBBI57 | LQQNEEKNHSDsstsEsEVssVsPLKNKHPDEDAVEAEGHE |
| Q9NY27 | S226 | Sugiyama | PPP4R2 SBBI57 | QNEEKNHSDsstsEsEVssVsPLKNKHPDEDAVEAEGHEVK |
| Q9NYB0 | S203 | Sugiyama | TERF2IP DRIP5 RAP1 PP8000 | RYLKHLRGQEHKyLLGDAPVsPssQKLKRKAEEDPEAADsG |
| Q9NYF3 | S255 | Sugiyama | FAM53C C5orf6 | PsLGPQASRFLPSARssPAssPELPWRPRGLRNLPRsRsQP |
| Q9NYF8 | S177 | Sugiyama | BCLAF1 BTF KIAA0164 | KRRGSQEKQTKKAEGEPQEEsPLKsKsQEEPKDtFEHDPsE |
| Q9NYF8 | S290 | Sugiyama | BCLAF1 BTF KIAA0164 | ERsGsGsVGNGssRysPsQNsPIHHIPsRRsPAKtIAPQNA |
| Q9NZB2 | T991 | Sugiyama | FAM120A C9orf10 KIAA0183 OSSA | PLQVVSVGGPARGRPRGVIstPVIRTFGRGGRYYGRGYKNQ |
| Q9NZH5 | S165 | SIGNOR|EPSD|PSP | PTTG2 | PLMILDEEGELEKLFQLGPPsPVKMPSPPWECNLLQSPSSI |
| Q9NZI6 | T177 | PSP | TFCP2L1 CRTR1 LBP9 | WDPAKRASAFIQVHCISTEFtPRKHGGEKGVPFRVQIDTFK |
| Q9NZJ0 | T429 | Sugiyama | DTL CDT2 CDW1 DCAF2 L2DTL RAMP | AsQKKKESRPGLVTVtssQstPAKAPRAKCNPsNssPssAA |
| Q9NZJ0 | T464 | EPSD|PSP | DTL CDT2 CDW1 DCAF2 L2DTL RAMP | sPssAACAPsCAGDLPLPsNtPtFsIKtsPAKARSPINRRG |
| Q9NZT2 | S378 | EPSD|PSP|Sugiyama | OGFR | LERsQGDEAGGHGEDRPEPLsPKEsKKRKLELSRREQPPTE |
| Q9P2E9 | S615 | Sugiyama | RRBP1 KIAA1398 | NQGKKTEsAsVQGRNTDVAQsPEAPKQEAPAKKKSGSKKKG |
| Q9UBF8 | S266 | EPSD|PSP | PI4KB PIK4CB | KPAHRKRELPsLsPAPDtGLsPsKRTHQRsKsDAtAsISLS |
| Q9UD71 | T75 | ELM | PPP1R1B DARPP32 | QRASGEGHHLKsKRPNPCAYtPPSLKAVQRIAESHLQSIsN |
| Q9UEY8 | S681 | Sugiyama | ADD3 ADDL | TIKsPEKIEEVLsPEGsPsKsPsKKKKKFRTPsFLKKNKKK |
| Q9UGL1 | S1328 | PSP | KDM5B JARID1B PLU1 RBBP2H1 | PGTTsFsLPDDWDNRTSYLHsPFSTGRSCIPLHGVSPEVNE |
| Q9UGL1 | S1456 | SIGNOR|PSP | KDM5B JARID1B PLU1 RBBP2H1 | KKIKLSHPKDMNNFKLERERsYELVRSAETHSLPSDTSYSE |
| Q9UGP4 | S272 | PSP | LIMD1 | GGRssEKPtGLWstASSQRVsPGLPsPNLENGAPAVGPVQP |
| Q9UGP4 | S277 | PSP | LIMD1 | EKPtGLWstASSQRVsPGLPsPNLENGAPAVGPVQPRtPsV |
| Q9UGP4 | S421 | PSP | LIMD1 | CKEGPLGWSSDGsLGsVLLDsPssPRVRLPCQPLVPGPELR |
| Q9UGP4 | S424 | PSP | LIMD1 | GPLGWSSDGsLGsVLLDsPssPRVRLPCQPLVPGPELRPSA |
| Q9UGV2 | S341 | Sugiyama | NDRG3 | MTRLARsRtHstsssLGsGEsPFsRsVtsNQsDGtQESCEs |
| Q9UI09 | T120 | SIGNOR|PSP | NDUFA12 DAP13 | TKPLTARKFIWTNHKFNVTGtPEQYVPYSTTRKKIQEWIPP |
| Q9UI09 | T142 | SIGNOR|PSP | NDUFA12 DAP13 | EQYVPYSTTRKKIQEWIPPStPYK_________________ |
| Q9UI10 | T86 | Sugiyama | EIF2B4 EIF2BD | AAQCQVGPTRELPESGIQLGtPREKVPAGRSKAELRAERRA |
| Q9UJ70 | S76 | EPSD|PSP | NAGK | AKRKAGVDPLVPLRsLGLsLsGGDQEDAGRILIEELRDRFP |
| Q9UJU6 | S232 | Sugiyama | DBNL CMAP SH3P7 PP5423 | RELREAARREQRyQEQGGEAsPQRtWEQQQEVVSRNRNEQE |
| Q9UJX2 | T562 | GPS6|EPSD|PSP | CDC23 ANAPC8 | tREEGKALLRQILQLRNQGEtPttEVPAPFFLPAsLsANNt |
| Q9UJX2 | T565 | SIGNOR|EPSD|PSP | CDC23 ANAPC8 | EGKALLRQILQLRNQGEtPttEVPAPFFLPAsLsANNtPtR |
| Q9UJX2 | T582 | GPS6|EPSD | CDC23 ANAPC8 | tPttEVPAPFFLPAsLsANNtPtRRVsPLNLssVtP_____ |
| Q9UJX5 | S779 | EPSD|PSP | ANAPC4 APC4 | DEEEEASNKPVKIKEEVLsEsEAENQQAGAAALAPEIVIKV |
| Q9UK13 | S238 | Sugiyama | ZNF221 | RVHMGEKCYKCDVCGKEFNQsSHLQTHQRVHTGEKPFKCGQ |
| Q9UK61 | T819 | PSP | TASOR C3orf63 FAM208A KIAA1105 | LsTDDAyEELRQKHEYELNstPDKKDYEQPTCAKVENAQFK |
| Q9UKA9 | S434 | Sugiyama | PTBP2 NPTB PTB PTBLP | TVQLPREGLDDQGLTKDFGNsPLHRFKKPGSKNFQNIFPPS |
| Q9UKX7 | S221 | SIGNOR|EPSD|PSP | NUP50 NPAP60L PRO1146 | HGNsGRNsESEsNKVAAEtQsPsLFGstKLQQEStFLFHGN |
| Q9ULC4 | S118 | GPS6|EPSD|PSP | MCTS1 MCT1 | DKGAIKFVLSGANIMCPGLtsPGAKLYPAAVDTIVAIMAEG |
| Q9ULW0 | S738 | EPSD|PSP | TPX2 C20orf1 C20orf2 DIL2 HCA519 | IRKYQGLEIKSSDQPLtVPVsPKFstRFHC___________ |
| Q9ULW0 | T72 | SIGNOR|EPSD|PSP | TPX2 C20orf1 C20orf2 DIL2 HCA519 | GGLFQGKtPLRKANLQQAIVtPLKPVDNtYYKEAEKENLVE |
| Q9UM11 | S151 | ELM | FZR1 CDH1 FYR FZR KIAA1242 | SLsTKRssPDDGNDVsPYsLsPVSNKSQKLLRsPRKPTRKI |
| Q9UM11 | S163 | ELM | FZR1 CDH1 FYR FZR KIAA1242 | NDVsPYsLsPVSNKSQKLLRsPRKPTRKISKIPFKVLDAPE |
| Q9UNE7 | S19 | Sugiyama | STUB1 CHIP PP1131 | __MKGKEEKEGGARLGAGGGsPEKsPsAQELKEQGNRLFVG |
| Q9UNE7 | S23 | Sugiyama | STUB1 CHIP PP1131 | GKEEKEGGARLGAGGGsPEKsPsAQELKEQGNRLFVGRKYP |
| Q9UNH5 | S411 | PSP | CDC14A | NGITQGDKLRALKSQRQPRTsPSCAFRSDDTKGHPRAVsQP |
| Q9UNH5 | S453 | PSP | CDC14A | RLSSSLQGSAVTLKTSKMALsPSATAKRINRTSLSSGATVR |
| Q9UNH5 | S549 | PSP | CDC14A | PELNNNQYNRSSNSNGGNLNsPPGPHSAKTEEHTTILRPSY |
| Q9UNX3 | S32 | Sugiyama | RPL26L1 RPL26P1 | sKNRKRHFNAPSHVRRKIMssPLSKELRQKYNVRSMPIRKD |
| Q9UNX3 | T8 | Sugiyama | RPL26L1 RPL26P1 | _____________MKFNPFVtsDRsKNRKRHFNAPSHVRRK |
| Q9UNZ2 | S140 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | NSFL1C UBXN2C | DDLFKGAKEHGAVAVERVTKsPGEtSKPRPFAGGGYRLGAA |
| Q9UPP1 | S120 | GPS6|EPSD|PSP | PHF8 KIAA1111 ZNF422 | KRRGSSKGHDTHKGKPVKTGsPTFVRELRSRTFDSSDEVIL |
| Q9UPP1 | S69 | GPS6|EPSD|PSP | PHF8 KIAA1111 ZNF422 | PYDVTRFMIECDMCQDWFHGsCVGVEEEKAADIDLYHCPNC |
| Q9UPT8 | S146 | Sugiyama | ZC3H4 C19orf7 KIAA1064 | HKRHAsSSDDFsDFsDDsDFsPSEKGHRKyREysPPyAPsH |
| Q9UPU5 | S1616 | SIGNOR|EPSD|PSP | USP24 KIAA1057 | LDDFLFRASRIILNsHsPAGsAAISQQDFHPKCSTANSRLA |
| Q9UPU5 | S2047 | SIGNOR|EPSD|PSP | USP24 KIAA1057 | VRRRYWNAYMLFYQRVSDQNsPVLPKKSRVSVVRQEAEDLs |
| Q9UPU5 | S2604 | SIGNOR|EPSD|PSP | USP24 KIAA1057 | GSEssPANENGDRHLQQGsEsPMMIGELRsDLDDVDP____ |
| Q9UQ35 | S1320 | Sugiyama | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | sMASSWGGPHFsPEHKELsNsPLRENsFGsPLEFRNsGPLG |
| Q9UQ35 | S1329 | Sugiyama | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | HFsPEHKELsNsPLRENsFGsPLEFRNsGPLGTEMNtGFss |
| Q9UQ35 | S1552 | Sugiyama | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | PLGQRsRsGssQELDVKPsAsPQERsEsDssPDSKAKTRTP |
| Q9UQ35 | S1658 | Sugiyama | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | SGSSSKGRGPsPEGssstEssPEHPPKSRTARRGsRSsPEP |
| Q9UQ35 | S2044 | Sugiyama | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | PAIRRRsRsRtPLLPRKRsRsRsPLAIRRRSRSRTPRTARG |
| Q9UQ35 | S2046 | Sugiyama | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | IRRRsRsRtPLLPRKRsRsRsPLAIRRRSRSRTPRTARGKR |
| Q9UQ35 | S2694 | Sugiyama | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | RSRSPRKPIDsLRDsRsLsysPVERRRPsPQPsPRDQQSSs |
| Q9UQ35 | T1413 | EPSD|PSP | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | KAGMssNQsIssPVLDAVPRtPsRERsssAssPEMKDGLPR |
| Q9UQ35 | T1655 | Sugiyama | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | RSRSGSSSKGRGPsPEGssstEssPEHPPKSRTARRGsRSs |
| Q9UQ35 | T866 | EPSD|PSP | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | sGtPPRQGsItsPQANEQsVtPQRRsCFEssPDPELKsRtP |
| Q9UQR0 | S267 | PSP | SCML2 | VKNIAKtEssPsEAsQHsMQsPQKTTLILPTQQVRRSSRIK |
| Q9UQR0 | S511 | EPSD|PSP | SCML2 | TERQstKRsPQQtVPYVVPLsPKLPKTKEYAsEGEPLFAGG |
| Q9UQR0 | S590 | EPSD|PSP | SCML2 | sQDFSRSVPGTTssPLVGDIsPKssPHEVKFQMQRKsEAPS |
| Q9UQR0 | T305 | EPSD|PSP | SCML2 | RIKPPGPTAVPKRSSSVKNItPRKKGPNSGKKEKPLPVICS |
| Q9Y2B0 | S65 | Sugiyama | CNPY2 MSAP TMEM4 ZSIG9 UNQ1943/PRO4426 | VDPKKTIQMGsFRINPDGsQsVVEVPyARsEAHLtELLEEI |
| Q9Y2I6 | S185 | SIGNOR|EPSD|PSP | NINL KIAA0980 NLP | QNELFEAQGQLQTWDSEDFGsPQKSCsPSFDTPESQIRGVW |
| Q9Y2I6 | S589 | SIGNOR|EPSD|PSP | NINL KIAA0980 NLP | QAELEGLWARLPKNRHsPSWsPDGRRRQLPGLGPAGISFLG |
| Q9Y2T7 | T124 | Sugiyama | YBX2 CSDA3 MSY2 | RNGyGFINRNDtKEDVFVHQtAIKRNNPRKFLRsVGDGEtV |
| Q9Y2V2 | S41 | Sugiyama | CARHSP1 | LDtPRsRERsPsPLRGNVVPsPLPtRRtRtFsAtVRASQGP |
| Q9Y2V2 | T23 | EPSD|PSP | CARHSP1 | sEPPPPPQPPtHQAsVGLLDtPRsRERsPsPLRGNVVPsPL |
| Q9Y2W1 | S243 | Sugiyama | THRAP3 BCLAF2 TRAP150 | WPDAtyGtGsAsRAsAVsELsPRERsPALKsPLQsVVVRRR |
| Q9Y2W2 | S237 | Sugiyama | WBP11 NPWBP SIPP1 SNP70 | RKVGFALDLPPRRRDEDMLysPELAQRGHDDDVSSTSEDDG |
| Q9Y2X3 | S514 | Sugiyama | NOP58 NOL5 NOP5 HSPC120 | KHIKEEPLsEEEPCtstAIAsPEKKKKKKKKRENED_____ |
| Q9Y3Z3 | T592 | SIGNOR|EPSD|PSP | SAMHD1 MOP5 | WCADRNFTKPQDGDVIAPLItPQKKEWNDstsVQNPtRLRE |
| Q9Y4H2 | S391 | EPSD|PSP | IRS2 | AAAGAAAAGARPVsVAGsPLsPGPVRAPLsRSHtLsGGCGG |
| Q9Y5N6 | T195 | EPSD|PSP | ORC6 ORC6L | LCKQLEKIGQQVDREPGDVAtPPRKRKKIVVEAPAKEMEKV |
| Q9Y5S2 | S1693 | Sugiyama | CDC42BPB KIAA1124 | stKHstPsNssNPsGPPsPNsPHRsQLPLEGLEQPACDT__ |
| Q9Y5T5 | S552 | SIGNOR|EPSD|PSP | USP16 MSTP039 | TEEVDMKNINMDNDLEVLtssPtRNLNGAYLTEGSNGEVDI |
| Q9Y673 | S62 | Sugiyama | ALG5 HSPC149 | EEKFFLNAKGQKETLPSIWDsPtKQLSVVVPSYNEEKRLPV |
| Q9Y6G9 | S207 | Sugiyama | DYNC1LI1 DNCLI1 | EQKLIRDFQEyVEPGEDFPAsPQRRNtAsQEDKDDsVVLPL |
| Q9Y6I3 | S382 | GPS6|SIGNOR|EPSD|PSP | EPN1 | GPSASDPWTPAPAFSDPWGGsPAKPSTNGTTAAGGFDTEPD |
| Q9Y6Q9 | S728 | SIGNOR|EPSD|PSP | NCOA3 AIB1 BHLHE42 RAC3 TRAM1 | KDTSSITSCGDGNVVKQEQLsPKKKENNALLRYLLDRDDPS |
| Q9Y6Q9 | S867 | EPSD|PSP | NCOA3 AIB1 BHLHE42 RAC3 TRAM1 | SIRPPYNRAVsLDsPVsVGssPPVKNISAFPMLPKQPMLGG |
| Q9Y6X9 | T717 | SIGNOR | MORC2 KIAA0852 ZCWCC1 | PsLLPNsKsPREVPSPKVIKtPVVKKtEsPIKLsPAtPsRK |
| Q9Y6X9 | T733 | SIGNOR | MORC2 KIAA0852 ZCWCC1 | KVIKtPVVKKtEsPIKLsPAtPsRKRsVAVsDEEEVEEEAE |
Site Promiscuity
Motif of predicted substrate sequence
Reactome pathways of predicted substrates
Download
| name | reactome_id | p | -log10p | ref_path | ref_path_lowest |
|---|---|---|---|---|---|
| Cell Cycle, Mitotic | R-HSA-69278 | 2.493561e-12 | 11.603 | 1 | 0 |
| Cell Cycle | R-HSA-1640170 | 1.160427e-11 | 10.935 | 1 | 0 |
| Chromatin organization | R-HSA-4839726 | 6.448808e-10 | 9.191 | 0 | 0 |
| Chromatin modifying enzymes | R-HSA-3247509 | 9.435086e-09 | 8.025 | 0 | 0 |
| Transcription of E2F targets under negative control by DREAM complex | R-HSA-1362277 | 2.544497e-08 | 7.594 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 9.836019e-08 | 7.007 | 1 | 0 |
| TP53 Regulates Transcription of Cell Cycle Genes | R-HSA-6791312 | 2.693041e-07 | 6.570 | 1 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 9.303307e-07 | 6.031 | 0 | 0 |
| PKMTs methylate histone lysines | R-HSA-3214841 | 9.193552e-07 | 6.037 | 0 | 0 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | R-HSA-1362300 | 1.754391e-06 | 5.756 | 1 | 1 |
| Formation of WDR5-containing histone-modifying complexes | R-HSA-9772755 | 1.848487e-06 | 5.733 | 0 | 0 |
| G1/S-Specific Transcription | R-HSA-69205 | 9.597116e-06 | 5.018 | 1 | 1 |
| Gene expression (Transcription) | R-HSA-74160 | 1.018514e-05 | 4.992 | 1 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 2.201207e-05 | 4.657 | 1 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 5.657221e-05 | 4.247 | 1 | 0 |
| Apoptotic execution phase | R-HSA-75153 | 5.656935e-05 | 4.247 | 0 | 0 |
| Formation of Senescence-Associated Heterochromatin Foci (SAHF) | R-HSA-2559584 | 6.078847e-05 | 4.216 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 6.306592e-05 | 4.200 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 9.712226e-05 | 4.013 | 0 | 0 |
| M Phase | R-HSA-68886 | 1.118064e-04 | 3.952 | 1 | 0 |
| Formation of the embryonic stem cell BAF (esBAF) complex | R-HSA-9933946 | 1.489120e-04 | 3.827 | 0 | 0 |
| Mitotic Spindle Checkpoint | R-HSA-69618 | 1.601031e-04 | 3.796 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 1.897826e-04 | 3.722 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | R-HSA-6804116 | 2.232591e-04 | 3.651 | 0 | 0 |
| Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | R-HSA-9934037 | 3.254552e-04 | 3.488 | 0 | 0 |
| ATP-dependent chromatin remodelers | R-HSA-9932444 | 5.505551e-04 | 3.259 | 0 | 0 |
| SWI/SNF chromatin remodelers | R-HSA-9932451 | 5.505551e-04 | 3.259 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 6.081267e-04 | 3.216 | 0 | 0 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | R-HSA-141444 | 7.641652e-04 | 3.117 | 0 | 0 |
| Amplification of signal from the kinetochores | R-HSA-141424 | 7.641652e-04 | 3.117 | 0 | 0 |
| TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | R-HSA-6804115 | 8.179089e-04 | 3.087 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 8.558659e-04 | 3.068 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 8.775908e-04 | 3.057 | 1 | 0 |
| S Phase | R-HSA-69242 | 9.035661e-04 | 3.044 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 9.922045e-04 | 3.003 | 1 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 1.004572e-03 | 2.998 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 1.004572e-03 | 2.998 | 0 | 0 |
| Apoptotic cleavage of cellular proteins | R-HSA-111465 | 1.015056e-03 | 2.994 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 1.078810e-03 | 2.967 | 1 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 1.129030e-03 | 2.947 | 1 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 1.269058e-03 | 2.897 | 1 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 1.310133e-03 | 2.883 | 0 | 0 |
| Deadenylation of mRNA | R-HSA-429947 | 1.407503e-03 | 2.852 | 0 | 0 |
| G1/S Transition | R-HSA-69206 | 1.438519e-03 | 2.842 | 1 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 1.460729e-03 | 2.835 | 1 | 0 |
| Activation of PUMA and translocation to mitochondria | R-HSA-139915 | 1.606725e-03 | 2.794 | 0 | 0 |
| Role of ABL in ROBO-SLIT signaling | R-HSA-428890 | 1.606725e-03 | 2.794 | 0 | 0 |
| Formation of the polybromo-BAF (pBAF) complex | R-HSA-9933939 | 1.919692e-03 | 2.717 | 0 | 0 |
| Transport of Mature Transcript to Cytoplasm | R-HSA-72202 | 2.092146e-03 | 2.679 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 2.217873e-03 | 2.654 | 0 | 0 |
| Cyclin D associated events in G1 | R-HSA-69231 | 2.283520e-03 | 2.641 | 0 | 0 |
| G1 Phase | R-HSA-69236 | 2.283520e-03 | 2.641 | 0 | 0 |
| Transport of Mature mRNAs Derived from Intronless Transcripts | R-HSA-159234 | 2.366169e-03 | 2.626 | 0 | 0 |
| Polo-like kinase mediated events | R-HSA-156711 | 2.416806e-03 | 2.617 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 2.633572e-03 | 2.579 | 0 | 0 |
| HATs acetylate histones | R-HSA-3214847 | 2.821722e-03 | 2.549 | 0 | 0 |
| RUNX1 regulates expression of components of tight junctions | R-HSA-8935964 | 3.269221e-03 | 2.486 | 0 | 0 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | R-HSA-9687136 | 3.617438e-03 | 2.442 | 0 | 0 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | R-HSA-8939243 | 3.631390e-03 | 2.440 | 0 | 0 |
| Cyclin A/B1/B2 associated events during G2/M transition | R-HSA-69273 | 3.631390e-03 | 2.440 | 1 | 1 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 3.923251e-03 | 2.406 | 0 | 0 |
| Caspase-mediated cleavage of cytoskeletal proteins | R-HSA-264870 | 3.917350e-03 | 2.407 | 0 | 0 |
| Regulation of endogenous retroelements | R-HSA-9842860 | 3.945386e-03 | 2.404 | 0 | 0 |
| Transport of the SLBP Dependant Mature mRNA | R-HSA-159230 | 4.416810e-03 | 2.355 | 0 | 0 |
| The CRY:PER:kinase complex represses transactivation by the BMAL:CLOCK (ARNTL:CLOCK) complex | R-HSA-9931521 | 4.815045e-03 | 2.317 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 4.818415e-03 | 2.317 | 0 | 0 |
| TFAP2A acts as a transcriptional repressor during retinoic acid induced cell differentiation | R-HSA-8869496 | 5.338335e-03 | 2.273 | 0 | 0 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | R-HSA-9659787 | 5.411220e-03 | 2.267 | 0 | 0 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | R-HSA-9661069 | 5.411220e-03 | 2.267 | 0 | 0 |
| Transport of Mature mRNA Derived from an Intronless Transcript | R-HSA-159231 | 5.090602e-03 | 2.293 | 0 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 5.493980e-03 | 2.260 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 6.150401e-03 | 2.211 | 1 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 7.027585e-03 | 2.153 | 1 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 8.618458e-03 | 2.065 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 9.173355e-03 | 2.037 | 1 | 1 |
| Transport of the SLBP independent Mature mRNA | R-HSA-159227 | 9.602998e-03 | 2.018 | 0 | 0 |
| DCC mediated attractive signaling | R-HSA-418885 | 9.603612e-03 | 2.018 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 1.002181e-02 | 1.999 | 1 | 1 |
| DNA Repair | R-HSA-73894 | 1.029546e-02 | 1.987 | 0 | 0 |
| Nuclear events stimulated by ALK signaling in cancer | R-HSA-9725371 | 1.031337e-02 | 1.987 | 0 | 0 |
| Activation of RAC1 | R-HSA-428540 | 1.104873e-02 | 1.957 | 0 | 0 |
| DNA Damage Bypass | R-HSA-73893 | 1.185592e-02 | 1.926 | 0 | 0 |
| Type I hemidesmosome assembly | R-HSA-446107 | 1.196762e-02 | 1.922 | 0 | 0 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | R-HSA-159236 | 1.241586e-02 | 1.906 | 0 | 0 |
| RUNX3 regulates RUNX1-mediated transcription | R-HSA-8951911 | 1.341588e-02 | 1.872 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 1.373085e-02 | 1.862 | 1 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 1.385775e-02 | 1.858 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 1.397359e-02 | 1.855 | 0 | 0 |
| Z-decay: degradation of maternal mRNAs by zygotically expressed factors | R-HSA-9820865 | 1.472397e-02 | 1.832 | 0 | 0 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | R-HSA-141405 | 1.578093e-02 | 1.802 | 0 | 0 |
| Inactivation of APC/C via direct inhibition of the APC/C complex | R-HSA-141430 | 1.578093e-02 | 1.802 | 0 | 0 |
| Nuclear Envelope Breakdown | R-HSA-2980766 | 1.567867e-02 | 1.805 | 1 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 1.488260e-02 | 1.827 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | R-HSA-6804114 | 1.578093e-02 | 1.802 | 1 | 1 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | R-HSA-6802955 | 1.725558e-02 | 1.763 | 0 | 0 |
| Signaling by moderate kinase activity BRAF mutants | R-HSA-6802946 | 1.725558e-02 | 1.763 | 0 | 0 |
| Signaling downstream of RAS mutants | R-HSA-9649948 | 1.725558e-02 | 1.763 | 0 | 0 |
| Signaling by RAS mutants | R-HSA-6802949 | 1.725558e-02 | 1.763 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 1.745993e-02 | 1.758 | 0 | 0 |
| HDR through MMEJ (alt-NHEJ) | R-HSA-5685939 | 1.917211e-02 | 1.717 | 0 | 0 |
| Formation of the non-canonical BAF (ncBAF) complex | R-HSA-9933947 | 1.917211e-02 | 1.717 | 0 | 0 |
| Initiation of Nuclear Envelope (NE) Reformation | R-HSA-2995383 | 1.931024e-02 | 1.714 | 1 | 1 |
| Phosphorylated BMAL1:CLOCK (ARNTL:CLOCK) activates expression of core clock genes | R-HSA-9931510 | 1.834081e-02 | 1.737 | 0 | 0 |
| FOXO-mediated transcription of cell cycle genes | R-HSA-9617828 | 1.931024e-02 | 1.714 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 1.797744e-02 | 1.745 | 0 | 0 |
| RET signaling | R-HSA-8853659 | 1.836968e-02 | 1.736 | 0 | 0 |
| Postmitotic nuclear pore complex (NPC) reformation | R-HSA-9615933 | 1.834081e-02 | 1.737 | 0 | 0 |
| Regulation of TP53 Activity through Association with Co-factors | R-HSA-6804759 | 1.917211e-02 | 1.717 | 0 | 0 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | R-HSA-176407 | 1.974432e-02 | 1.705 | 0 | 0 |
| Nuclear Receptor transcription pathway | R-HSA-383280 | 2.108220e-02 | 1.676 | 0 | 0 |
| Signaling by high-kinase activity BRAF mutants | R-HSA-6802948 | 2.127715e-02 | 1.672 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 2.288482e-02 | 1.640 | 0 | 0 |
| Oncogenic MAPK signaling | R-HSA-6802957 | 2.257524e-02 | 1.646 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 2.158213e-02 | 1.666 | 0 | 0 |
| Positive Regulation of CDH1 Gene Transcription | R-HSA-9764790 | 2.271104e-02 | 1.644 | 0 | 0 |
| Apoptosis induced DNA fragmentation | R-HSA-140342 | 2.271104e-02 | 1.644 | 0 | 0 |
| Homology Directed Repair | R-HSA-5693538 | 2.292635e-02 | 1.640 | 0 | 0 |
| Regulation of MECP2 expression and activity | R-HSA-9022692 | 2.347106e-02 | 1.629 | 0 | 0 |
| Loss of MECP2 binding ability to 5mC-DNA | R-HSA-9022538 | 2.398110e-02 | 1.620 | 0 | 0 |
| FOXO-mediated transcription of cell death genes | R-HSA-9614657 | 2.435445e-02 | 1.613 | 0 | 0 |
| Formation of the canonical BAF (cBAF) complex | R-HSA-9933937 | 2.445772e-02 | 1.612 | 0 | 0 |
| Loss of MECP2 binding ability to 5hmC-DNA | R-HSA-9022534 | 2.524780e-02 | 1.598 | 0 | 0 |
| Nuclear Envelope (NE) Reassembly | R-HSA-2995410 | 2.562112e-02 | 1.591 | 1 | 0 |
| DNA Damage/Telomere Stress Induced Senescence | R-HSA-2559586 | 2.772767e-02 | 1.557 | 0 | 0 |
| Constitutive Signaling by AKT1 E17K in Cancer | R-HSA-5674400 | 2.785129e-02 | 1.555 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 2.905280e-02 | 1.537 | 0 | 0 |
| E2F mediated regulation of DNA replication | R-HSA-113510 | 2.965367e-02 | 1.528 | 1 | 0 |
| RAF activation | R-HSA-5673000 | 3.138805e-02 | 1.503 | 0 | 0 |
| Nuclear import of Rev protein | R-HSA-180746 | 3.138805e-02 | 1.503 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 3.164680e-02 | 1.500 | 0 | 0 |
| Interactions of Rev with host cellular proteins | R-HSA-177243 | 3.201835e-02 | 1.495 | 0 | 0 |
| SHOC2 M1731 mutant abolishes MRAS complex function | R-HSA-9726840 | 3.528305e-02 | 1.452 | 0 | 0 |
| Recognition of DNA damage by PCNA-containing replication complex | R-HSA-110314 | 3.297435e-02 | 1.482 | 0 | 0 |
| Activation of the pre-replicative complex | R-HSA-68962 | 3.495341e-02 | 1.457 | 0 | 0 |
| Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) | R-HSA-5619107 | 3.495341e-02 | 1.457 | 0 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 3.560552e-02 | 1.448 | 0 | 0 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 3.308611e-02 | 1.480 | 0 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 3.342754e-02 | 1.476 | 0 | 0 |
| Nuclear Pore Complex (NPC) Disassembly | R-HSA-3301854 | 3.598001e-02 | 1.444 | 1 | 1 |
| Resolution of Abasic Sites (AP sites) | R-HSA-73933 | 3.632901e-02 | 1.440 | 0 | 0 |
| M-decay: degradation of maternal mRNAs by maternally stored factors | R-HSA-9820841 | 3.632901e-02 | 1.440 | 0 | 0 |
| RUNX3 regulates BCL2L11 (BIM) transcription | R-HSA-8952158 | 3.794864e-02 | 1.421 | 0 | 0 |
| Inhibition of replication initiation of damaged DNA by RB1/E2F1 | R-HSA-113501 | 3.829145e-02 | 1.417 | 0 | 0 |
| Phosphorylation of CLOCK, acetylation of BMAL1 (ARNTL) at target gene promoters | R-HSA-9931512 | 3.829145e-02 | 1.417 | 0 | 0 |
| Deadenylation-dependent mRNA decay | R-HSA-429914 | 3.880387e-02 | 1.411 | 0 | 0 |
| IP3 and IP4 transport between cytosol and nucleus | R-HSA-1855196 | 4.034001e-02 | 1.394 | 0 | 0 |
| IP6 and IP7 transport between cytosol and nucleus | R-HSA-1855229 | 4.034001e-02 | 1.394 | 0 | 0 |
| MAP2K and MAPK activation | R-HSA-5674135 | 4.103085e-02 | 1.387 | 0 | 0 |
| Signaling by RAF1 mutants | R-HSA-9656223 | 4.103085e-02 | 1.387 | 0 | 0 |
| Transcriptional Regulation by MECP2 | R-HSA-8986944 | 4.166138e-02 | 1.380 | 0 | 0 |
| Disorders of Developmental Biology | R-HSA-9675151 | 4.584971e-02 | 1.339 | 0 | 0 |
| APC-Cdc20 mediated degradation of Nek2A | R-HSA-179409 | 4.246220e-02 | 1.372 | 0 | 0 |
| Vpr-mediated nuclear import of PICs | R-HSA-180910 | 4.651930e-02 | 1.332 | 0 | 0 |
| RNA Polymerase I Transcription Initiation | R-HSA-73762 | 4.613755e-02 | 1.336 | 0 | 0 |
| MTOR signalling | R-HSA-165159 | 4.613755e-02 | 1.336 | 0 | 0 |
| Deactivation of the beta-catenin transactivating complex | R-HSA-3769402 | 4.651930e-02 | 1.332 | 0 | 0 |
| Signaling by MRAS-complex mutants | R-HSA-9660537 | 4.708614e-02 | 1.327 | 0 | 0 |
| Gain-of-function MRAS complexes activate RAF signaling | R-HSA-9726842 | 4.708614e-02 | 1.327 | 0 | 0 |
| RNA Polymerase II Transcription Termination | R-HSA-73856 | 4.729670e-02 | 1.325 | 0 | 0 |
| RUNX3 regulates NOTCH signaling | R-HSA-8941856 | 4.803517e-02 | 1.318 | 0 | 0 |
| Signaling by PDGFR in disease | R-HSA-9671555 | 5.002798e-02 | 1.301 | 0 | 0 |
| Breakdown of the nuclear lamina | R-HSA-352238 | 5.249165e-02 | 1.280 | 0 | 0 |
| Rev-mediated nuclear export of HIV RNA | R-HSA-165054 | 5.249645e-02 | 1.280 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in BCR signaling | R-HSA-8939245 | 5.521897e-02 | 1.258 | 0 | 0 |
| Signaling by membrane-tethered fusions of PDGFRA or PDGFRB | R-HSA-9673768 | 5.521897e-02 | 1.258 | 0 | 0 |
| IPs transport between nucleus and cytosol | R-HSA-1855170 | 5.273448e-02 | 1.278 | 0 | 0 |
| Expression of BMAL (ARNTL), CLOCK, and NPAS2 | R-HSA-9931509 | 5.896165e-02 | 1.229 | 0 | 0 |
| mTORC1-mediated signalling | R-HSA-166208 | 5.839495e-02 | 1.234 | 0 | 0 |
| Signaling by EGFR | R-HSA-177929 | 5.401960e-02 | 1.267 | 0 | 0 |
| Frs2-mediated activation | R-HSA-170968 | 5.911393e-02 | 1.228 | 0 | 0 |
| Interleukin-6 signaling | R-HSA-1059683 | 5.911393e-02 | 1.228 | 0 | 0 |
| Downregulation of TGF-beta receptor signaling | R-HSA-2173788 | 5.839495e-02 | 1.234 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 5.719848e-02 | 1.243 | 0 | 0 |
| Regulation of Glucokinase by Glucokinase Regulatory Protein | R-HSA-170822 | 5.977171e-02 | 1.224 | 0 | 0 |
| ALK mutants bind TKIs | R-HSA-9700645 | 6.081552e-02 | 1.216 | 0 | 0 |
| AKT phosphorylates targets in the nucleus | R-HSA-198693 | 6.081552e-02 | 1.216 | 0 | 0 |
| Regulation of CDH11 gene transcription | R-HSA-9762293 | 6.081552e-02 | 1.216 | 0 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 6.319180e-02 | 1.199 | 1 | 1 |
| Regulation of MITF-M-dependent genes involved in pigmentation | R-HSA-9824585 | 6.400122e-02 | 1.194 | 0 | 0 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 6.454330e-02 | 1.190 | 1 | 1 |
| Signaling by cytosolic FGFR1 fusion mutants | R-HSA-1839117 | 6.505225e-02 | 1.187 | 0 | 0 |
| Ephrin signaling | R-HSA-3928664 | 6.505225e-02 | 1.187 | 0 | 0 |
| Interactions of Vpr with host cellular proteins | R-HSA-176033 | 6.592436e-02 | 1.181 | 0 | 0 |
| RUNX3 regulates CDKN1A transcription | R-HSA-8941855 | 7.557692e-02 | 1.122 | 0 | 0 |
| Epithelial-Mesenchymal Transition (EMT) during gastrulation | R-HSA-9758919 | 7.557692e-02 | 1.122 | 0 | 0 |
| CDC6 association with the ORC:origin complex | R-HSA-68689 | 7.557692e-02 | 1.122 | 0 | 0 |
| Loss of MECP2 binding ability to the NCoR/SMRT complex | R-HSA-9022537 | 7.557692e-02 | 1.122 | 0 | 0 |
| Establishment of Sister Chromatid Cohesion | R-HSA-2468052 | 7.642663e-02 | 1.117 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Cyclin B | R-HSA-174048 | 7.617673e-02 | 1.118 | 1 | 1 |
| mRNA 3'-end processing | R-HSA-72187 | 6.807109e-02 | 1.167 | 0 | 0 |
| Signaling by BRAF and RAF1 fusions | R-HSA-6802952 | 6.798929e-02 | 1.168 | 0 | 0 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 7.605779e-02 | 1.119 | 1 | 1 |
| Receptor Mediated Mitophagy | R-HSA-8934903 | 7.642663e-02 | 1.117 | 0 | 0 |
| Negative feedback regulation of MAPK pathway | R-HSA-5674499 | 7.557692e-02 | 1.122 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 7.536343e-02 | 1.123 | 0 | 0 |
| Oncogene Induced Senescence | R-HSA-2559585 | 7.557625e-02 | 1.122 | 0 | 0 |
| Constitutive Signaling by NOTCH1 t(7;9)(NOTCH1:M1580_K2555) Translocation Mutant | R-HSA-2660826 | 7.557692e-02 | 1.122 | 0 | 0 |
| Signaling by NOTCH1 t(7;9)(NOTCH1:M1580_K2555) Translocation Mutant | R-HSA-2660825 | 7.557692e-02 | 1.122 | 0 | 0 |
| Signalling to ERKs | R-HSA-187687 | 7.557625e-02 | 1.122 | 0 | 0 |
| Transcriptional Regulation by VENTX | R-HSA-8853884 | 7.339170e-02 | 1.134 | 0 | 0 |
| Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | R-HSA-9845323 | 7.784481e-02 | 1.109 | 0 | 0 |
| Negative Regulation of CDH1 Gene Transcription | R-HSA-9764725 | 7.784481e-02 | 1.109 | 0 | 0 |
| Signaling by FGFR1 in disease | R-HSA-5655302 | 8.136828e-02 | 1.090 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 8.161085e-02 | 1.088 | 0 | 0 |
| Cell-extracellular matrix interactions | R-HSA-446353 | 8.525373e-02 | 1.069 | 0 | 0 |
| NGF-stimulated transcription | R-HSA-9031628 | 8.584864e-02 | 1.066 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 8.682840e-02 | 1.061 | 0 | 0 |
| TGFBR3 expression | R-HSA-9839394 | 8.838533e-02 | 1.054 | 0 | 0 |
| Centrosome maturation | R-HSA-380287 | 8.863757e-02 | 1.052 | 1 | 0 |
| SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | R-HSA-2173796 | 9.371609e-02 | 1.028 | 0 | 0 |
| Drug resistance of PDGFR mutants | R-HSA-9674415 | 1.146589e-01 | 0.941 | 0 | 0 |
| PDGFR mutants bind TKIs | R-HSA-9674428 | 1.146589e-01 | 0.941 | 0 | 0 |
| Sorafenib-resistant PDGFR mutants | R-HSA-9674404 | 1.146589e-01 | 0.941 | 0 | 0 |
| Defective translocation of RB1 mutants to the nucleus | R-HSA-9661070 | 1.146589e-01 | 0.941 | 0 | 0 |
| APC truncation mutants are not K63 polyubiquitinated | R-HSA-5467333 | 1.146589e-01 | 0.941 | 0 | 0 |
| Regorafenib-resistant PDGFR mutants | R-HSA-9674403 | 1.146589e-01 | 0.941 | 0 | 0 |
| Sunitinib-resistant PDGFR mutants | R-HSA-9674401 | 1.146589e-01 | 0.941 | 0 | 0 |
| Imatinib-resistant PDGFR mutants | R-HSA-9674396 | 1.146589e-01 | 0.941 | 0 | 0 |
| Alternative Lengthening of Telomeres (ALT) | R-HSA-9006821 | 2.161771e-01 | 0.665 | 0 | 0 |
| Defective Inhibition of DNA Recombination at Telomere | R-HSA-9670621 | 2.161771e-01 | 0.665 | 0 | 0 |
| Diseases of Telomere Maintenance | R-HSA-9673013 | 2.161771e-01 | 0.665 | 0 | 0 |
| Impaired BRCA2 translocation to the nucleus | R-HSA-9709275 | 2.161771e-01 | 0.665 | 0 | 0 |
| Impaired BRCA2 binding to SEM1 (DSS1) | R-HSA-9763198 | 2.161771e-01 | 0.665 | 0 | 0 |
| Defective Mismatch Repair Associated With MLH1 | R-HSA-5545483 | 2.161771e-01 | 0.665 | 0 | 0 |
| Defective Inhibition of DNA Recombination at Telomere Due to DAXX Mutations | R-HSA-9670613 | 2.161771e-01 | 0.665 | 0 | 0 |
| Defective Mismatch Repair Associated With PMS2 | R-HSA-5632987 | 2.161771e-01 | 0.665 | 0 | 0 |
| Defective Inhibition of DNA Recombination at Telomere Due to ATRX Mutations | R-HSA-9670615 | 2.161771e-01 | 0.665 | 0 | 0 |
| MET interacts with TNS proteins | R-HSA-8875513 | 1.248181e-01 | 0.904 | 0 | 0 |
| Loss of Function of KMT2D in Kabuki Syndrome | R-HSA-9944971 | 1.248181e-01 | 0.904 | 0 | 0 |
| Loss of Function of KMT2D in MLL4 Complex Formation in Kabuki Syndrome | R-HSA-9944997 | 1.248181e-01 | 0.904 | 0 | 0 |
| Regulation of gap junction activity | R-HSA-191650 | 1.665160e-01 | 0.779 | 0 | 0 |
| MECP2 regulates transcription of genes involved in GABA signaling | R-HSA-9022927 | 1.665160e-01 | 0.779 | 0 | 0 |
| Inhibition of TSC complex formation by PKB | R-HSA-165181 | 1.665160e-01 | 0.779 | 0 | 0 |
| Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes | R-HSA-69200 | 1.665160e-01 | 0.779 | 0 | 0 |
| Signaling by MAP2K mutants | R-HSA-9652169 | 1.665160e-01 | 0.779 | 0 | 0 |
| Nef mediated downregulation of CD28 cell surface expression | R-HSA-164939 | 3.060599e-01 | 0.514 | 0 | 0 |
| SMAD4 MH2 Domain Mutants in Cancer | R-HSA-3311021 | 3.060599e-01 | 0.514 | 0 | 0 |
| Defective VWF binding to collagen type I | R-HSA-9845622 | 3.060599e-01 | 0.514 | 0 | 0 |
| Loss of Function of SMAD4 in Cancer | R-HSA-3304347 | 3.060599e-01 | 0.514 | 0 | 0 |
| SMAD2/3 MH2 Domain Mutants in Cancer | R-HSA-3315487 | 3.060599e-01 | 0.514 | 0 | 0 |
| Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG) | R-HSA-5619101 | 3.060599e-01 | 0.514 | 0 | 0 |
| Defective SLC9A9 causes autism 16 (AUTS16) | R-HSA-5619052 | 3.060599e-01 | 0.514 | 0 | 0 |
| Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG) | R-HSA-5660686 | 3.060599e-01 | 0.514 | 0 | 0 |
| Cohesin Loading onto Chromatin | R-HSA-2470946 | 1.243392e-01 | 0.905 | 0 | 0 |
| SOS-mediated signalling | R-HSA-112412 | 1.243392e-01 | 0.905 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in interleukin signaling | R-HSA-8939247 | 2.101609e-01 | 0.677 | 0 | 0 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 2.101609e-01 | 0.677 | 0 | 0 |
| IRS activation | R-HSA-74713 | 2.101609e-01 | 0.677 | 0 | 0 |
| G2 Phase | R-HSA-68911 | 2.101609e-01 | 0.677 | 0 | 0 |
| Loss of phosphorylation of MECP2 at T308 | R-HSA-9022535 | 2.101609e-01 | 0.677 | 0 | 0 |
| Formation of annular gap junctions | R-HSA-196025 | 1.520406e-01 | 0.818 | 0 | 0 |
| Phosphorylation of the APC/C | R-HSA-176412 | 1.002573e-01 | 0.999 | 1 | 1 |
| Regulation of FOXO transcriptional activity by acetylation | R-HSA-9617629 | 1.336058e-01 | 0.874 | 0 | 0 |
| Pervasive developmental disorders | R-HSA-9005895 | 1.336058e-01 | 0.874 | 0 | 0 |
| Disorders of Nervous System Development | R-HSA-9697154 | 1.336058e-01 | 0.874 | 0 | 0 |
| Loss of function of MECP2 in Rett syndrome | R-HSA-9005891 | 1.336058e-01 | 0.874 | 0 | 0 |
| Gap junction degradation | R-HSA-190873 | 1.814640e-01 | 0.741 | 0 | 0 |
| MAPK1 (ERK2) activation | R-HSA-112411 | 1.814640e-01 | 0.741 | 0 | 0 |
| Phosphorylation of Emi1 | R-HSA-176417 | 2.547590e-01 | 0.594 | 1 | 1 |
| Synthesis of PS | R-HSA-1483101 | 2.547590e-01 | 0.594 | 0 | 0 |
| PTK6 Regulates Cell Cycle | R-HSA-8849470 | 2.547590e-01 | 0.594 | 0 | 0 |
| Signaling by RNF43 mutants | R-HSA-5340588 | 2.547590e-01 | 0.594 | 0 | 0 |
| Drug resistance in ERBB2 KD mutants | R-HSA-9665230 | 3.856403e-01 | 0.414 | 0 | 0 |
| Drug-mediated inhibition of ERBB2 signaling | R-HSA-9652282 | 3.856403e-01 | 0.414 | 0 | 0 |
| MPS IIIC - Sanfilippo syndrome C | R-HSA-2206291 | 3.856403e-01 | 0.414 | 0 | 0 |
| Defective PAPSS2 causes SEMD-PA | R-HSA-3560796 | 3.856403e-01 | 0.414 | 0 | 0 |
| Resistance of ERBB2 KD mutants to neratinib | R-HSA-9665246 | 3.856403e-01 | 0.414 | 0 | 0 |
| Resistance of ERBB2 KD mutants to lapatinib | R-HSA-9665251 | 3.856403e-01 | 0.414 | 0 | 0 |
| Resistance of ERBB2 KD mutants to tesevatinib | R-HSA-9665245 | 3.856403e-01 | 0.414 | 0 | 0 |
| Defective VWF cleavage by ADAMTS13 variant | R-HSA-9845621 | 3.856403e-01 | 0.414 | 0 | 0 |
| Resistance of ERBB2 KD mutants to trastuzumab | R-HSA-9665233 | 3.856403e-01 | 0.414 | 0 | 0 |
| Resistance of ERBB2 KD mutants to afatinib | R-HSA-9665249 | 3.856403e-01 | 0.414 | 0 | 0 |
| Glycogen storage disease type 0 (muscle GYS1) | R-HSA-3828062 | 3.856403e-01 | 0.414 | 0 | 0 |
| Resistance of ERBB2 KD mutants to AEE788 | R-HSA-9665250 | 3.856403e-01 | 0.414 | 0 | 0 |
| Enhanced cleavage of VWF variant by ADAMTS13 | R-HSA-9845619 | 3.856403e-01 | 0.414 | 0 | 0 |
| Defective OPLAH causes OPLAHD | R-HSA-5578998 | 3.856403e-01 | 0.414 | 0 | 0 |
| Resistance of ERBB2 KD mutants to sapitinib | R-HSA-9665244 | 3.856403e-01 | 0.414 | 0 | 0 |
| Glycogen storage disease type XV (GYG1) | R-HSA-3814836 | 3.856403e-01 | 0.414 | 0 | 0 |
| Drug resistance in ERBB2 TMD/JMD mutants | R-HSA-9665737 | 3.856403e-01 | 0.414 | 0 | 0 |
| Resistance of ERBB2 KD mutants to osimertinib | R-HSA-9665247 | 3.856403e-01 | 0.414 | 0 | 0 |
| Defective POMT2 causes MDDGA2, MDDGB2 and MDDGC2 | R-HSA-5083629 | 3.856403e-01 | 0.414 | 0 | 0 |
| Defective POMT1 causes MDDGA1, MDDGB1 and MDDGC1 | R-HSA-5083633 | 3.856403e-01 | 0.414 | 0 | 0 |
| MECP2 regulates transcription of neuronal ligands | R-HSA-9022702 | 2.122456e-01 | 0.673 | 0 | 0 |
| MET activates RAP1 and RAC1 | R-HSA-8875555 | 2.122456e-01 | 0.673 | 0 | 0 |
| MAPK3 (ERK1) activation | R-HSA-110056 | 2.122456e-01 | 0.673 | 1 | 1 |
| Activation of Ca-permeable Kainate Receptor | R-HSA-451308 | 2.122456e-01 | 0.673 | 0 | 0 |
| Regulation of CDH1 mRNA translation by microRNAs | R-HSA-9764562 | 1.789909e-01 | 0.747 | 0 | 0 |
| Signaling by LTK in cancer | R-HSA-9842640 | 2.995182e-01 | 0.524 | 0 | 0 |
| G2/M DNA replication checkpoint | R-HSA-69478 | 2.995182e-01 | 0.524 | 1 | 1 |
| E2F-enabled inhibition of pre-replication complex formation | R-HSA-113507 | 2.995182e-01 | 0.524 | 1 | 1 |
| MECP2 regulates neuronal receptors and channels | R-HSA-9022699 | 1.000053e-01 | 1.000 | 0 | 0 |
| Notch-HLH transcription pathway | R-HSA-350054 | 1.305230e-01 | 0.884 | 0 | 0 |
| Regulation of localization of FOXO transcription factors | R-HSA-9614399 | 2.440368e-01 | 0.613 | 0 | 0 |
| Processive synthesis on the lagging strand | R-HSA-69183 | 2.033802e-01 | 0.692 | 0 | 0 |
| Translesion synthesis by REV1 | R-HSA-110312 | 2.033802e-01 | 0.692 | 0 | 0 |
| Translesion Synthesis by POLH | R-HSA-110320 | 1.717857e-01 | 0.765 | 0 | 0 |
| Impaired BRCA2 binding to PALB2 | R-HSA-9709603 | 1.717857e-01 | 0.765 | 0 | 0 |
| Impaired BRCA2 binding to RAD51 | R-HSA-9709570 | 1.395247e-01 | 0.855 | 0 | 0 |
| Processing of Capped Intronless Pre-mRNA | R-HSA-75067 | 1.631265e-01 | 0.787 | 0 | 0 |
| Defective homologous recombination repair (HRR) due to PALB2 loss of function | R-HSA-9701193 | 1.921360e-01 | 0.716 | 0 | 0 |
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA2/RAD51/RAD51C binding function | R-HSA-9704646 | 1.921360e-01 | 0.716 | 0 | 0 |
| Defective HDR through Homologous Recombination Repair (HRR) due to PALB2 loss of BRCA1 binding function | R-HSA-9704331 | 1.921360e-01 | 0.716 | 0 | 0 |
| Defective homologous recombination repair (HRR) due to BRCA1 loss of function | R-HSA-9701192 | 1.921360e-01 | 0.716 | 0 | 0 |
| Translesion synthesis by POLI | R-HSA-5656121 | 2.286703e-01 | 0.641 | 0 | 0 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | R-HSA-354194 | 2.286703e-01 | 0.641 | 0 | 0 |
| MECP2 regulates transcription factors | R-HSA-9022707 | 3.438156e-01 | 0.464 | 0 | 0 |
| Signaling by cytosolic PDGFRA and PDGFRB fusion proteins | R-HSA-9673766 | 4.560986e-01 | 0.341 | 0 | 0 |
| Signaling by plasma membrane FGFR1 fusions | R-HSA-8853336 | 4.560986e-01 | 0.341 | 0 | 0 |
| Invadopodia formation | R-HSA-8941237 | 4.560986e-01 | 0.341 | 0 | 0 |
| MET activates PTPN11 | R-HSA-8865999 | 4.560986e-01 | 0.341 | 0 | 0 |
| Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | R-HSA-9843970 | 1.323667e-01 | 0.878 | 0 | 0 |
| Defective homologous recombination repair (HRR) due to BRCA2 loss of function | R-HSA-9701190 | 1.323667e-01 | 0.878 | 0 | 0 |
| Lagging Strand Synthesis | R-HSA-69186 | 2.132822e-01 | 0.671 | 0 | 0 |
| Processing of Intronless Pre-mRNAs | R-HSA-77595 | 2.546880e-01 | 0.594 | 0 | 0 |
| Translesion synthesis by POLK | R-HSA-5655862 | 2.546880e-01 | 0.594 | 0 | 0 |
| Regulation of RUNX1 Expression and Activity | R-HSA-8934593 | 1.988056e-01 | 0.702 | 0 | 0 |
| RUNX3 regulates p14-ARF | R-HSA-8951936 | 3.093685e-01 | 0.510 | 0 | 0 |
| Polymerase switching | R-HSA-69091 | 3.093685e-01 | 0.510 | 0 | 0 |
| Leading Strand Synthesis | R-HSA-69109 | 3.093685e-01 | 0.510 | 0 | 0 |
| Gap-filling DNA repair synthesis and ligation in GG-NER | R-HSA-5696397 | 2.351205e-01 | 0.629 | 0 | 0 |
| p130Cas linkage to MAPK signaling for integrins | R-HSA-372708 | 2.812634e-01 | 0.551 | 0 | 0 |
| SLBP Dependent Processing of Replication-Dependent Histone Pre-mRNAs | R-HSA-77588 | 3.871689e-01 | 0.412 | 0 | 0 |
| Regulation of TBK1, IKKε-mediated activation of IRF3, IRF7 upon TLR3 ligation | R-HSA-9828211 | 3.871689e-01 | 0.412 | 0 | 0 |
| Regulation of NPAS4 mRNA translation | R-HSA-9768778 | 3.871689e-01 | 0.412 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 1.245702e-01 | 0.905 | 1 | 1 |
| Gap-filling DNA repair synthesis and ligation in TC-NER | R-HSA-6782210 | 1.637766e-01 | 0.786 | 0 | 0 |
| Deposition of new CENPA-containing nucleosomes at the centromere | R-HSA-606279 | 2.027219e-01 | 0.693 | 0 | 0 |
| Nucleosome assembly | R-HSA-774815 | 2.027219e-01 | 0.693 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 1.636180e-01 | 0.786 | 1 | 1 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 1.636180e-01 | 0.786 | 1 | 1 |
| Processing of DNA double-strand break ends | R-HSA-5693607 | 1.338433e-01 | 0.873 | 0 | 0 |
| Removal of the Flap Intermediate | R-HSA-69166 | 3.751729e-01 | 0.426 | 0 | 0 |
| HCN channels | R-HSA-1296061 | 5.184800e-01 | 0.285 | 0 | 0 |
| AKT-mediated inactivation of FOXO1A | R-HSA-211163 | 5.184800e-01 | 0.285 | 0 | 0 |
| TGFBR1 KD Mutants in Cancer | R-HSA-3656532 | 5.184800e-01 | 0.285 | 0 | 0 |
| Signaling by LRP5 mutants | R-HSA-5339717 | 5.184800e-01 | 0.285 | 0 | 0 |
| GRB7 events in ERBB2 signaling | R-HSA-1306955 | 5.184800e-01 | 0.285 | 0 | 0 |
| Defective LFNG causes SCDO3 | R-HSA-5083630 | 5.184800e-01 | 0.285 | 0 | 0 |
| snRNP Assembly | R-HSA-191859 | 1.998248e-01 | 0.699 | 0 | 0 |
| Metabolism of non-coding RNA | R-HSA-194441 | 1.998248e-01 | 0.699 | 0 | 0 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | R-HSA-174178 | 2.151316e-01 | 0.667 | 0 | 0 |
| Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA) | R-HSA-5693554 | 3.272848e-01 | 0.485 | 0 | 0 |
| HDACs deacetylate histones | R-HSA-3214815 | 2.433006e-01 | 0.614 | 0 | 0 |
| Erythropoietin activates RAS | R-HSA-9027284 | 4.076644e-01 | 0.390 | 0 | 0 |
| Signaling by PDGFRA extracellular domain mutants | R-HSA-9673770 | 4.076644e-01 | 0.390 | 0 | 0 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | R-HSA-9673767 | 4.076644e-01 | 0.390 | 0 | 0 |
| Transcription-Coupled Nucleotide Excision Repair (TC-NER) | R-HSA-6781827 | 2.182781e-01 | 0.661 | 0 | 0 |
| Regulation of endogenous retroelements by KRAB-ZFP proteins | R-HSA-9843940 | 2.474853e-01 | 0.606 | 0 | 0 |
| Activation of PPARGC1A (PGC-1alpha) by phosphorylation | R-HSA-2151209 | 4.696760e-01 | 0.328 | 0 | 0 |
| DNA replication initiation | R-HSA-68952 | 4.696760e-01 | 0.328 | 0 | 0 |
| Interaction between L1 and Ankyrins | R-HSA-445095 | 3.748185e-01 | 0.426 | 0 | 0 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | R-HSA-73779 | 3.493313e-01 | 0.457 | 0 | 0 |
| Condensation of Prophase Chromosomes | R-HSA-2299718 | 3.382880e-01 | 0.471 | 1 | 1 |
| mRNA Splicing - Minor Pathway | R-HSA-72165 | 3.382880e-01 | 0.471 | 0 | 0 |
| RNA Polymerase III Transcription Initiation From Type 2 Promoter | R-HSA-76066 | 4.170675e-01 | 0.380 | 0 | 0 |
| Ras activation upon Ca2+ influx through NMDA receptor | R-HSA-442982 | 4.170675e-01 | 0.380 | 0 | 0 |
| RNA polymerase II transcribes snRNA genes | R-HSA-6807505 | 2.734645e-01 | 0.563 | 0 | 0 |
| Dual Incision in GG-NER | R-HSA-5696400 | 3.827955e-01 | 0.417 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 2.984631e-01 | 0.525 | 1 | 1 |
| RNA Polymerase II HIV Promoter Escape | R-HSA-167162 | 3.884126e-01 | 0.411 | 0 | 0 |
| HIV Transcription Initiation | R-HSA-167161 | 3.884126e-01 | 0.411 | 0 | 0 |
| RNA Polymerase II Transcription Initiation | R-HSA-75953 | 3.884126e-01 | 0.411 | 0 | 0 |
| NOTCH3 Activation and Transmission of Signal to the Nucleus | R-HSA-9013507 | 4.438619e-01 | 0.353 | 0 | 0 |
| Regulation of CDH11 mRNA translation by microRNAs | R-HSA-9759811 | 5.083696e-01 | 0.294 | 0 | 0 |
| SMAD2/3 Phosphorylation Motif Mutants in Cancer | R-HSA-3304356 | 5.737099e-01 | 0.241 | 0 | 0 |
| FLT3 signaling by CBL mutants | R-HSA-9706377 | 5.737099e-01 | 0.241 | 0 | 0 |
| Enhanced binding of GP1BA variant to VWF multimer:collagen | R-HSA-9845620 | 5.737099e-01 | 0.241 | 0 | 0 |
| Defective binding of VWF variant to GPIb:IX:V | R-HSA-9846298 | 5.737099e-01 | 0.241 | 0 | 0 |
| PRC2 methylates histones and DNA | R-HSA-212300 | 4.255131e-01 | 0.371 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 3.694813e-01 | 0.432 | 1 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 3.694813e-01 | 0.432 | 1 | 0 |
| RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | R-HSA-167160 | 4.702687e-01 | 0.328 | 0 | 0 |
| RNA Pol II CTD phosphorylation and interaction with CE | R-HSA-77075 | 4.702687e-01 | 0.328 | 0 | 0 |
| RNA Polymerase II Promoter Escape | R-HSA-73776 | 4.275539e-01 | 0.369 | 0 | 0 |
| Dual incision in TC-NER | R-HSA-6782135 | 4.126814e-01 | 0.384 | 0 | 0 |
| EGFR downregulation | R-HSA-182971 | 4.691085e-01 | 0.329 | 0 | 0 |
| Formation of RNA Pol II elongation complex | R-HSA-112382 | 4.469719e-01 | 0.350 | 0 | 0 |
| Anchoring fibril formation | R-HSA-2214320 | 5.451670e-01 | 0.263 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 5.451670e-01 | 0.263 | 1 | 1 |
| Regulation of TBK1, IKKε (IKBKE)-mediated activation of IRF3, IRF7 | R-HSA-9824878 | 5.451670e-01 | 0.263 | 0 | 0 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance | R-HSA-76042 | 4.663796e-01 | 0.331 | 0 | 0 |
| RNA Polymerase II Transcription Elongation | R-HSA-75955 | 4.649823e-01 | 0.333 | 0 | 0 |
| COPI-dependent Golgi-to-ER retrograde traffic | R-HSA-6811434 | 4.302978e-01 | 0.366 | 0 | 0 |
| GAB1 signalosome | R-HSA-180292 | 5.308988e-01 | 0.275 | 0 | 0 |
| PCNA-Dependent Long Patch Base Excision Repair | R-HSA-5651801 | 5.308988e-01 | 0.275 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 4.828674e-01 | 0.316 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Securin | R-HSA-174154 | 5.045504e-01 | 0.297 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 5.005951e-01 | 0.301 | 1 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 5.181351e-01 | 0.286 | 1 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 5.594251e-01 | 0.252 | 0 | 0 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | R-HSA-9027276 | 5.799941e-01 | 0.237 | 0 | 0 |
| Defects of platelet adhesion to exposed collagen | R-HSA-9823587 | 6.226079e-01 | 0.206 | 0 | 0 |
| PDE3B signalling | R-HSA-165160 | 6.226079e-01 | 0.206 | 0 | 0 |
| Loss of Function of SMAD2/3 in Cancer | R-HSA-3304349 | 6.226079e-01 | 0.206 | 0 | 0 |
| SLIT2:ROBO1 increases RHOA activity | R-HSA-8985586 | 6.226079e-01 | 0.206 | 0 | 0 |
| PKB-mediated events | R-HSA-109703 | 6.226079e-01 | 0.206 | 0 | 0 |
| Noncanonical activation of NOTCH3 | R-HSA-9017802 | 6.226079e-01 | 0.206 | 0 | 0 |
| Signaling by MAPK mutants | R-HSA-9652817 | 6.226079e-01 | 0.206 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 5.405999e-01 | 0.267 | 0 | 0 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | R-HSA-9609523 | 5.868766e-01 | 0.231 | 0 | 0 |
| HSF1-dependent transactivation | R-HSA-3371571 | 5.777803e-01 | 0.238 | 0 | 0 |
| RUNX1 and FOXP3 control the development of regulatory T lymphocytes (Tregs) | R-HSA-8877330 | 6.128187e-01 | 0.213 | 0 | 0 |
| CD28 dependent Vav1 pathway | R-HSA-389359 | 6.128187e-01 | 0.213 | 0 | 0 |
| Golgi Cisternae Pericentriolar Stack Reorganization | R-HSA-162658 | 6.128187e-01 | 0.213 | 1 | 1 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | R-HSA-75035 | 6.128187e-01 | 0.213 | 1 | 1 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 5.952663e-01 | 0.225 | 1 | 1 |
| RNA Polymerase III Abortive And Retractive Initiation | R-HSA-749476 | 6.002521e-01 | 0.222 | 0 | 0 |
| NOTCH4 Intracellular Domain Regulates Transcription | R-HSA-9013695 | 6.132056e-01 | 0.212 | 0 | 0 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 6.123754e-01 | 0.213 | 1 | 0 |
| B-WICH complex positively regulates rRNA expression | R-HSA-5250924 | 6.123754e-01 | 0.213 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 6.179947e-01 | 0.209 | 1 | 1 |
| Signaling by Erythropoietin | R-HSA-9006335 | 6.162696e-01 | 0.210 | 0 | 0 |
| Late endosomal microautophagy | R-HSA-9615710 | 6.162696e-01 | 0.210 | 0 | 0 |
| Formation of TC-NER Pre-Incision Complex | R-HSA-6781823 | 6.422938e-01 | 0.192 | 0 | 0 |
| Autodegradation of Cdh1 by Cdh1:APC/C | R-HSA-174084 | 6.422938e-01 | 0.192 | 0 | 0 |
| activated TAK1 mediates p38 MAPK activation | R-HSA-450302 | 6.383802e-01 | 0.195 | 0 | 0 |
| Unblocking of NMDA receptors, glutamate binding and activation | R-HSA-438066 | 6.383802e-01 | 0.195 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in WNT signaling | R-HSA-8939256 | 6.658995e-01 | 0.177 | 0 | 0 |
| Activation of NIMA Kinases NEK9, NEK6, NEK7 | R-HSA-2980767 | 6.658995e-01 | 0.177 | 1 | 1 |
| STAT5 Activation | R-HSA-9645135 | 6.658995e-01 | 0.177 | 0 | 0 |
| Erythropoietin activates STAT5 | R-HSA-9027283 | 6.658995e-01 | 0.177 | 0 | 0 |
| Autointegration results in viral DNA circles | R-HSA-177539 | 6.658995e-01 | 0.177 | 0 | 0 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | R-HSA-9670439 | 6.623823e-01 | 0.179 | 0 | 0 |
| Competing endogenous RNAs (ceRNAs) regulate PTEN translation | R-HSA-8948700 | 6.724913e-01 | 0.172 | 0 | 0 |
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | R-HSA-450385 | 6.724913e-01 | 0.172 | 0 | 0 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | R-HSA-2173791 | 6.724913e-01 | 0.172 | 0 | 0 |
| Transcription of the HIV genome | R-HSA-167172 | 4.462510e-01 | 0.350 | 0 | 0 |
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | R-HSA-110313 | 2.347887e-01 | 0.629 | 0 | 0 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 3.401851e-01 | 0.468 | 0 | 0 |
| Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | R-HSA-9818564 | 6.337804e-01 | 0.198 | 0 | 0 |
| Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | R-HSA-9851695 | 6.337804e-01 | 0.198 | 0 | 0 |
| MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis | R-HSA-9841922 | 6.337804e-01 | 0.198 | 0 | 0 |
| Signaling by NOTCH3 | R-HSA-9012852 | 5.005951e-01 | 0.301 | 0 | 0 |
| FOXO-mediated transcription | R-HSA-9614085 | 2.718867e-01 | 0.566 | 0 | 0 |
| FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | R-HSA-9615017 | 3.884126e-01 | 0.411 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 2.015227e-01 | 0.696 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 1.568514e-01 | 0.805 | 0 | 0 |
| Nucleotide Excision Repair | R-HSA-5696398 | 1.307851e-01 | 0.883 | 0 | 0 |
| Integrin signaling | R-HSA-354192 | 1.082807e-01 | 0.965 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 3.107157e-01 | 0.508 | 0 | 0 |
| NOTCH3 Intracellular Domain Regulates Transcription | R-HSA-9013508 | 4.458340e-01 | 0.351 | 0 | 0 |
| mRNA Capping | R-HSA-72086 | 6.162696e-01 | 0.210 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 3.102415e-01 | 0.508 | 0 | 0 |
| POLB-Dependent Long Patch Base Excision Repair | R-HSA-110362 | 1.129433e-01 | 0.947 | 0 | 0 |
| RNA Polymerase I Promoter Clearance | R-HSA-73854 | 3.293566e-01 | 0.482 | 0 | 0 |
| VxPx cargo-targeting to cilium | R-HSA-5620916 | 5.868766e-01 | 0.231 | 0 | 0 |
| GP1b-IX-V activation signalling | R-HSA-430116 | 1.814640e-01 | 0.741 | 0 | 0 |
| Termination of translesion DNA synthesis | R-HSA-5656169 | 4.223113e-01 | 0.374 | 0 | 0 |
| p75NTR recruits signalling complexes | R-HSA-209543 | 5.799941e-01 | 0.237 | 0 | 0 |
| RNA Polymerase III Transcription | R-HSA-74158 | 6.002521e-01 | 0.222 | 0 | 0 |
| Transcriptional Regulation by E2F6 | R-HSA-8953750 | 1.141788e-01 | 0.942 | 0 | 0 |
| Constitutive Signaling by Overexpressed ERBB2 | R-HSA-9634285 | 3.093685e-01 | 0.510 | 0 | 0 |
| MAPK6/MAPK4 signaling | R-HSA-5687128 | 4.596300e-01 | 0.338 | 1 | 1 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | R-HSA-5693565 | 1.998248e-01 | 0.699 | 0 | 0 |
| Assembly of the pre-replicative complex | R-HSA-68867 | 4.861071e-01 | 0.313 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 4.777994e-01 | 0.321 | 0 | 0 |
| DNA strand elongation | R-HSA-69190 | 3.189290e-01 | 0.496 | 0 | 0 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | R-HSA-8862803 | 1.631265e-01 | 0.787 | 0 | 0 |
| Neurodegenerative Diseases | R-HSA-8863678 | 1.631265e-01 | 0.787 | 0 | 0 |
| Regulation of HSF1-mediated heat shock response | R-HSA-3371453 | 1.554325e-01 | 0.808 | 0 | 0 |
| Positive epigenetic regulation of rRNA expression | R-HSA-5250913 | 2.606138e-01 | 0.584 | 0 | 0 |
| RNA Polymerase I Transcription | R-HSA-73864 | 3.579192e-01 | 0.446 | 0 | 0 |
| Energy dependent regulation of mTOR by LKB1-AMPK | R-HSA-380972 | 4.458340e-01 | 0.351 | 0 | 0 |
| Synthesis of PIPs at the late endosome membrane | R-HSA-1660517 | 5.013632e-01 | 0.300 | 0 | 0 |
| Platelet Aggregation (Plug Formation) | R-HSA-76009 | 2.027219e-01 | 0.693 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 2.088977e-01 | 0.680 | 0 | 0 |
| Global Genome Nucleotide Excision Repair (GG-NER) | R-HSA-5696399 | 1.605620e-01 | 0.794 | 0 | 0 |
| Formation of the posterior neural plate | R-HSA-9832991 | 2.440368e-01 | 0.613 | 0 | 0 |
| HDR through Single Strand Annealing (SSA) | R-HSA-5685938 | 2.019525e-01 | 0.695 | 0 | 0 |
| Interleukin receptor SHC signaling | R-HSA-912526 | 2.804503e-01 | 0.552 | 0 | 0 |
| Transcriptional regulation of testis differentiation | R-HSA-9690406 | 4.709035e-01 | 0.327 | 0 | 0 |
| Telomere C-strand (Lagging Strand) Synthesis | R-HSA-174417 | 5.492674e-01 | 0.260 | 0 | 0 |
| Meiotic synapsis | R-HSA-1221632 | 6.123754e-01 | 0.213 | 0 | 0 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | R-HSA-5693567 | 9.733526e-02 | 1.012 | 0 | 0 |
| COPII-mediated vesicle transport | R-HSA-204005 | 6.084681e-01 | 0.216 | 0 | 0 |
| RUNX3 regulates WNT signaling | R-HSA-8951430 | 1.243392e-01 | 0.905 | 0 | 0 |
| Regulation of cytoskeletal remodeling and cell spreading by IPP complex components | R-HSA-446388 | 2.547590e-01 | 0.594 | 0 | 0 |
| PI3K/AKT activation | R-HSA-198203 | 2.122456e-01 | 0.673 | 0 | 0 |
| Activated NTRK3 signals through PI3K | R-HSA-9603381 | 3.438156e-01 | 0.464 | 0 | 0 |
| DNA Damage Recognition in GG-NER | R-HSA-5696394 | 2.190279e-01 | 0.660 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 1.952408e-01 | 0.709 | 0 | 0 |
| Transcriptional regulation by small RNAs | R-HSA-5578749 | 2.739756e-01 | 0.562 | 0 | 0 |
| Formation of Incision Complex in GG-NER | R-HSA-5696395 | 3.493313e-01 | 0.457 | 0 | 0 |
| RNA Polymerase III Transcription Initiation From Type 1 Promoter | R-HSA-76061 | 4.438619e-01 | 0.353 | 0 | 0 |
| CRMPs in Sema3A signaling | R-HSA-399956 | 6.436421e-01 | 0.191 | 0 | 0 |
| Signaling by Activin | R-HSA-1502540 | 6.724913e-01 | 0.172 | 0 | 0 |
| Defective Intrinsic Pathway for Apoptosis | R-HSA-9734009 | 2.176397e-01 | 0.662 | 0 | 0 |
| Resolution of AP sites via the multiple-nucleotide patch replacement pathway | R-HSA-110373 | 1.988056e-01 | 0.702 | 0 | 0 |
| Signaling by CSF1 (M-CSF) in myeloid cells | R-HSA-9680350 | 3.827955e-01 | 0.417 | 0 | 0 |
| Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | R-HSA-2173793 | 1.637766e-01 | 0.786 | 0 | 0 |
| Activation of ATR in response to replication stress | R-HSA-176187 | 1.082807e-01 | 0.965 | 0 | 0 |
| Diseases of DNA Double-Strand Break Repair | R-HSA-9675136 | 1.323667e-01 | 0.878 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 2.704035e-01 | 0.568 | 0 | 0 |
| DNA Double Strand Break Response | R-HSA-5693606 | 3.096975e-01 | 0.509 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 3.503576e-01 | 0.455 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 5.385237e-01 | 0.269 | 0 | 0 |
| RNA Polymerase III Transcription Initiation | R-HSA-76046 | 6.380325e-01 | 0.195 | 0 | 0 |
| p75NTR signals via NF-kB | R-HSA-193639 | 6.724913e-01 | 0.172 | 0 | 0 |
| Activated NOTCH1 Transmits Signal to the Nucleus | R-HSA-2122948 | 3.510124e-01 | 0.455 | 0 | 0 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | R-HSA-2894858 | 3.185936e-01 | 0.497 | 0 | 0 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | R-HSA-2644602 | 3.185936e-01 | 0.497 | 0 | 0 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | R-HSA-2894862 | 3.185936e-01 | 0.497 | 0 | 0 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | R-HSA-2644606 | 3.185936e-01 | 0.497 | 0 | 0 |
| Dopamine receptors | R-HSA-390651 | 1.665160e-01 | 0.779 | 0 | 0 |
| Mitotic Telophase/Cytokinesis | R-HSA-68884 | 1.129433e-01 | 0.947 | 0 | 0 |
| Negative regulation of MET activity | R-HSA-6807004 | 1.921360e-01 | 0.716 | 0 | 0 |
| NOSTRIN mediated eNOS trafficking | R-HSA-203641 | 3.438156e-01 | 0.464 | 0 | 0 |
| RAF-independent MAPK1/3 activation | R-HSA-112409 | 2.575452e-01 | 0.589 | 1 | 0 |
| TFAP2 (AP-2) family regulates transcription of cell cycle factors | R-HSA-8866911 | 5.184800e-01 | 0.285 | 0 | 0 |
| Telomere C-strand synthesis initiation | R-HSA-174430 | 4.076644e-01 | 0.390 | 0 | 0 |
| IRS-related events triggered by IGF1R | R-HSA-2428928 | 3.342654e-01 | 0.476 | 0 | 0 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | R-HSA-427389 | 5.091443e-01 | 0.293 | 0 | 0 |
| Retrograde transport at the Trans-Golgi-Network | R-HSA-6811440 | 5.045504e-01 | 0.297 | 0 | 0 |
| GLI proteins bind promoters of Hh responsive genes to promote transcription | R-HSA-5635851 | 6.226079e-01 | 0.206 | 0 | 0 |
| RNA Polymerase I Transcription Termination | R-HSA-73863 | 5.703763e-01 | 0.244 | 0 | 0 |
| PINK1-PRKN Mediated Mitophagy | R-HSA-5205685 | 5.937077e-01 | 0.226 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 6.380325e-01 | 0.195 | 0 | 0 |
| Mitophagy | R-HSA-5205647 | 2.365945e-01 | 0.626 | 0 | 0 |
| Nuclear RNA decay | R-HSA-9930044 | 1.082807e-01 | 0.965 | 0 | 0 |
| TICAM1-dependent activation of IRF3/IRF7 | R-HSA-9013973 | 5.451670e-01 | 0.263 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 5.308988e-01 | 0.275 | 0 | 0 |
| Fanconi Anemia Pathway | R-HSA-6783310 | 6.246279e-01 | 0.204 | 0 | 0 |
| Assembly of collagen fibrils and other multimeric structures | R-HSA-2022090 | 4.297041e-01 | 0.367 | 0 | 0 |
| Senescence-Associated Secretory Phenotype (SASP) | R-HSA-2559582 | 5.356584e-01 | 0.271 | 0 | 0 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | R-HSA-5617472 | 6.546026e-01 | 0.184 | 0 | 0 |
| Activation of HOX genes during differentiation | R-HSA-5619507 | 6.546026e-01 | 0.184 | 0 | 0 |
| Signaling by NOTCH1 | R-HSA-1980143 | 3.293566e-01 | 0.482 | 0 | 0 |
| Signal attenuation | R-HSA-74749 | 2.122456e-01 | 0.673 | 0 | 0 |
| NoRC negatively regulates rRNA expression | R-HSA-427413 | 1.089292e-01 | 0.963 | 0 | 0 |
| Presynaptic phase of homologous DNA pairing and strand exchange | R-HSA-5693616 | 2.546002e-01 | 0.594 | 0 | 0 |
| Activated NTRK2 signals through FRS2 and FRS3 | R-HSA-9028731 | 5.799941e-01 | 0.237 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 4.269856e-01 | 0.370 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 4.804181e-01 | 0.318 | 0 | 0 |
| HDR through Homologous Recombination (HRR) | R-HSA-5685942 | 3.096975e-01 | 0.509 | 0 | 0 |
| Interleukin-6 family signaling | R-HSA-6783589 | 3.037311e-01 | 0.518 | 0 | 0 |
| RNA Polymerase II Pre-transcription Events | R-HSA-674695 | 2.066169e-01 | 0.685 | 0 | 0 |
| EGR2 and SOX10-mediated initiation of Schwann cell myelination | R-HSA-9619665 | 5.368076e-01 | 0.270 | 0 | 0 |
| MET activates RAS signaling | R-HSA-8851805 | 3.093685e-01 | 0.510 | 0 | 0 |
| Homologous DNA Pairing and Strand Exchange | R-HSA-5693579 | 1.877954e-01 | 0.726 | 0 | 0 |
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | R-HSA-5358565 | 5.013632e-01 | 0.300 | 0 | 0 |
| Synthesis of PIPs at the early endosome membrane | R-HSA-1660516 | 3.272848e-01 | 0.485 | 0 | 0 |
| Resolution of D-Loop Structures | R-HSA-5693537 | 3.614135e-01 | 0.442 | 0 | 0 |
| Signaling by NOTCH1 in Cancer | R-HSA-2644603 | 3.185936e-01 | 0.497 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 1.255359e-01 | 0.901 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 4.058064e-01 | 0.392 | 0 | 0 |
| Prolonged ERK activation events | R-HSA-169893 | 1.002573e-01 | 0.999 | 0 | 0 |
| Neurexins and neuroligins | R-HSA-6794361 | 3.115076e-01 | 0.507 | 0 | 0 |
| Insulin receptor signalling cascade | R-HSA-74751 | 5.136502e-01 | 0.289 | 0 | 0 |
| Late Phase of HIV Life Cycle | R-HSA-162599 | 1.284229e-01 | 0.891 | 0 | 0 |
| Oxidative Stress Induced Senescence | R-HSA-2559580 | 2.230988e-01 | 0.652 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 2.768679e-01 | 0.558 | 1 | 0 |
| Resolution of AP sites via the single-nucleotide replacement pathway | R-HSA-110381 | 2.101609e-01 | 0.677 | 0 | 0 |
| Calcineurin activates NFAT | R-HSA-2025928 | 1.814640e-01 | 0.741 | 0 | 0 |
| PTK6 Expression | R-HSA-8849473 | 3.438156e-01 | 0.464 | 0 | 0 |
| Constitutive Signaling by NOTCH1 HD Domain Mutants | R-HSA-2691232 | 3.093685e-01 | 0.510 | 0 | 0 |
| Signaling by NOTCH1 HD Domain Mutants in Cancer | R-HSA-2691230 | 3.093685e-01 | 0.510 | 0 | 0 |
| Negative epigenetic regulation of rRNA expression | R-HSA-5250941 | 1.255359e-01 | 0.901 | 0 | 0 |
| RORA,B,C and NR1D1 (REV-ERBA) regulate gene expression | R-HSA-9933387 | 2.772803e-01 | 0.557 | 0 | 0 |
| G2/M DNA damage checkpoint | R-HSA-69473 | 2.066169e-01 | 0.685 | 1 | 0 |
| Resolution of D-loop Structures through Holliday Junction Intermediates | R-HSA-5693568 | 3.401020e-01 | 0.468 | 0 | 0 |
| CD163 mediating an anti-inflammatory response | R-HSA-9662834 | 5.083696e-01 | 0.294 | 0 | 0 |
| PTK6 Down-Regulation | R-HSA-8849472 | 5.737099e-01 | 0.241 | 0 | 0 |
| Post-transcriptional silencing by small RNAs | R-HSA-426496 | 5.737099e-01 | 0.241 | 0 | 0 |
| IRS-mediated signalling | R-HSA-112399 | 3.956501e-01 | 0.403 | 0 | 0 |
| RAB GEFs exchange GTP for GDP on RABs | R-HSA-8876198 | 3.609007e-01 | 0.443 | 0 | 0 |
| Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | R-HSA-5358606 | 5.013632e-01 | 0.300 | 0 | 0 |
| G2/M Checkpoints | R-HSA-69481 | 3.715613e-01 | 0.430 | 1 | 0 |
| Polymerase switching on the C-strand of the telomere | R-HSA-174411 | 5.215684e-01 | 0.283 | 0 | 0 |
| SLC15A4:TASL-dependent IRF5 activation | R-HSA-9860276 | 6.226079e-01 | 0.206 | 0 | 0 |
| NOTCH1 Intracellular Domain Regulates Transcription | R-HSA-2122947 | 5.417687e-01 | 0.266 | 0 | 0 |
| Antigen processing: Ubiquitination & Proteasome degradation | R-HSA-983168 | 5.077238e-01 | 0.294 | 0 | 0 |
| Signaling by NODAL | R-HSA-1181150 | 5.868766e-01 | 0.231 | 0 | 0 |
| TNFR1-induced proapoptotic signaling | R-HSA-5357786 | 6.132056e-01 | 0.212 | 0 | 0 |
| RUNX3 regulates YAP1-mediated transcription | R-HSA-8951671 | 6.658995e-01 | 0.177 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 3.956394e-01 | 0.403 | 0 | 0 |
| Negative regulation of MAPK pathway | R-HSA-5675221 | 3.884126e-01 | 0.411 | 0 | 0 |
| IGF1R signaling cascade | R-HSA-2428924 | 3.819940e-01 | 0.418 | 0 | 0 |
| Mismatch Repair | R-HSA-5358508 | 5.308988e-01 | 0.275 | 0 | 0 |
| Regulation of TP53 Activity through Acetylation | R-HSA-6804758 | 1.082807e-01 | 0.965 | 0 | 0 |
| Negative regulation of FGFR3 signaling | R-HSA-5654732 | 5.937077e-01 | 0.226 | 0 | 0 |
| IL-6-type cytokine receptor ligand interactions | R-HSA-6788467 | 6.128187e-01 | 0.213 | 0 | 0 |
| Negative regulation of FGFR4 signaling | R-HSA-5654733 | 6.162696e-01 | 0.210 | 0 | 0 |
| FGFR1 mutant receptor activation | R-HSA-1839124 | 2.019525e-01 | 0.695 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 1.534796e-01 | 0.814 | 0 | 0 |
| Cardiogenesis | R-HSA-9733709 | 1.082807e-01 | 0.965 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 4.614508e-01 | 0.336 | 0 | 0 |
| E3 ubiquitin ligases ubiquitinate target proteins | R-HSA-8866654 | 5.952663e-01 | 0.225 | 0 | 0 |
| InlB-mediated entry of Listeria monocytogenes into host cell | R-HSA-8875360 | 6.724913e-01 | 0.172 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 4.444298e-01 | 0.352 | 0 | 0 |
| Formation of the beta-catenin:TCF transactivating complex | R-HSA-201722 | 1.141962e-01 | 0.942 | 0 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 4.275539e-01 | 0.369 | 0 | 0 |
| Signaling by FLT3 fusion proteins | R-HSA-9703465 | 1.988056e-01 | 0.702 | 0 | 0 |
| Signaling by FGFR4 | R-HSA-5654743 | 5.878410e-01 | 0.231 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 4.588270e-01 | 0.338 | 0 | 0 |
| Signaling by LTK | R-HSA-9842663 | 1.336058e-01 | 0.874 | 0 | 0 |
| Transcriptional activation of cell cycle inhibitor p21 | R-HSA-69895 | 5.184800e-01 | 0.285 | 0 | 0 |
| Transcriptional activation of p53 responsive genes | R-HSA-69560 | 5.184800e-01 | 0.285 | 0 | 0 |
| p38MAPK events | R-HSA-171007 | 4.076644e-01 | 0.390 | 0 | 0 |
| Dopamine Neurotransmitter Release Cycle | R-HSA-212676 | 4.438619e-01 | 0.353 | 0 | 0 |
| LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production | R-HSA-3134973 | 5.737099e-01 | 0.241 | 0 | 0 |
| Negative regulation of TCF-dependent signaling by WNT ligand antagonists | R-HSA-3772470 | 5.451670e-01 | 0.263 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 2.636904e-01 | 0.579 | 0 | 0 |
| Estrogen-dependent nuclear events downstream of ESR-membrane signaling | R-HSA-9634638 | 4.702687e-01 | 0.328 | 0 | 0 |
| Signaling by FGFR3 | R-HSA-5654741 | 6.246279e-01 | 0.204 | 0 | 0 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | R-HSA-2404192 | 3.980469e-01 | 0.400 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 6.175560e-01 | 0.209 | 1 | 0 |
| Rap1 signalling | R-HSA-392517 | 3.354392e-01 | 0.474 | 0 | 0 |
| Activation of gene expression by SREBF (SREBP) | R-HSA-2426168 | 4.971095e-01 | 0.304 | 0 | 0 |
| Repression of WNT target genes | R-HSA-4641265 | 5.799941e-01 | 0.237 | 0 | 0 |
| Selective autophagy | R-HSA-9663891 | 5.170871e-01 | 0.286 | 0 | 0 |
| Mitochondrial unfolded protein response (UPRmt) | R-HSA-9841251 | 5.703763e-01 | 0.244 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex in Cancer | R-HSA-3304351 | 6.658995e-01 | 0.177 | 0 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 5.044743e-01 | 0.297 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 6.334054e-01 | 0.198 | 0 | 0 |
| Transcriptional activation of mitochondrial biogenesis | R-HSA-2151201 | 4.013826e-01 | 0.396 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 1.892460e-01 | 0.723 | 1 | 0 |
| Regulation of cholesterol biosynthesis by SREBP (SREBF) | R-HSA-1655829 | 2.674823e-01 | 0.573 | 0 | 0 |
| APEX1-Independent Resolution of AP Sites via the Single Nucleotide Replacement Pathway | R-HSA-5649702 | 1.814640e-01 | 0.741 | 0 | 0 |
| HIV Life Cycle | R-HSA-162587 | 1.306803e-01 | 0.884 | 0 | 0 |
| Regulation of NPAS4 gene expression | R-HSA-9768759 | 2.812634e-01 | 0.551 | 0 | 0 |
| Spry regulation of FGF signaling | R-HSA-1295596 | 4.076644e-01 | 0.390 | 0 | 0 |
| Protein-protein interactions at synapses | R-HSA-6794362 | 2.492154e-01 | 0.603 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 4.164367e-01 | 0.380 | 0 | 0 |
| Synthesis of PIPs at the Golgi membrane | R-HSA-1660514 | 5.463140e-01 | 0.263 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 4.466875e-01 | 0.350 | 0 | 0 |
| Rab regulation of trafficking | R-HSA-9007101 | 2.530689e-01 | 0.597 | 0 | 0 |
| Listeria monocytogenes entry into host cells | R-HSA-8876384 | 6.383802e-01 | 0.195 | 0 | 0 |
| Negative regulators of DDX58/IFIH1 signaling | R-HSA-936440 | 6.589744e-01 | 0.181 | 0 | 0 |
| Regulation of PTEN gene transcription | R-HSA-8943724 | 1.328047e-01 | 0.877 | 0 | 0 |
| TP53 Regulates Transcription of DNA Repair Genes | R-HSA-6796648 | 1.098430e-01 | 0.959 | 0 | 0 |
| HDMs demethylate histones | R-HSA-3214842 | 3.272848e-01 | 0.485 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 4.793535e-01 | 0.319 | 0 | 0 |
| Signaling by VEGF | R-HSA-194138 | 6.337804e-01 | 0.198 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 5.796461e-01 | 0.237 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 6.033826e-01 | 0.219 | 0 | 0 |
| Formation of editosomes by ADAR proteins | R-HSA-77042 | 2.161771e-01 | 0.665 | 0 | 0 |
| Binding of TCF/LEF:CTNNB1 to target gene promoters | R-HSA-4411364 | 1.243392e-01 | 0.905 | 0 | 0 |
| Sodium/Proton exchangers | R-HSA-425986 | 1.520406e-01 | 0.818 | 0 | 0 |
| mRNA Editing: A to I Conversion | R-HSA-75064 | 3.856403e-01 | 0.414 | 0 | 0 |
| Regulation of cortical dendrite branching | R-HSA-8985801 | 3.856403e-01 | 0.414 | 0 | 0 |
| Localization of the PINCH-ILK-PARVIN complex to focal adhesions | R-HSA-446343 | 3.856403e-01 | 0.414 | 0 | 0 |
| C6 deamination of adenosine | R-HSA-75102 | 3.856403e-01 | 0.414 | 0 | 0 |
| TGFBR3 regulates activin signaling | R-HSA-9839406 | 3.856403e-01 | 0.414 | 0 | 0 |
| Ionotropic activity of kainate receptors | R-HSA-451306 | 2.440368e-01 | 0.613 | 0 | 0 |
| Cation-coupled Chloride cotransporters | R-HSA-426117 | 3.438156e-01 | 0.464 | 0 | 0 |
| Negative regulation of TCF-dependent signaling by DVL-interacting proteins | R-HSA-5368598 | 4.560986e-01 | 0.341 | 0 | 0 |
| NEP/NS2 Interacts with the Cellular Export Machinery | R-HSA-168333 | 2.027219e-01 | 0.693 | 0 | 0 |
| SARS-CoV-2 targets PDZ proteins in cell-cell junction | R-HSA-9705677 | 5.184800e-01 | 0.285 | 0 | 0 |
| RUNX2 regulates genes involved in differentiation of myeloid cells | R-HSA-8941333 | 5.184800e-01 | 0.285 | 0 | 0 |
| Kinesins | R-HSA-983189 | 2.125588e-01 | 0.673 | 0 | 0 |
| Signalling to RAS | R-HSA-167044 | 3.899877e-01 | 0.409 | 0 | 0 |
| Differentiation of naive CD+ T cells to T helper 1 cells (Th1 cells) | R-HSA-9942503 | 4.396269e-01 | 0.357 | 0 | 0 |
| Differentiation of T cells | R-HSA-9945266 | 4.396269e-01 | 0.357 | 0 | 0 |
| Viral Messenger RNA Synthesis | R-HSA-168325 | 3.342654e-01 | 0.476 | 0 | 0 |
| Loss of Function of TGFBR1 in Cancer | R-HSA-3656534 | 5.737099e-01 | 0.241 | 0 | 0 |
| PI3K Cascade | R-HSA-109704 | 4.107125e-01 | 0.386 | 0 | 0 |
| Regulation of FZD by ubiquitination | R-HSA-4641263 | 5.013632e-01 | 0.300 | 0 | 0 |
| Budding and maturation of HIV virion | R-HSA-162588 | 4.691085e-01 | 0.329 | 0 | 0 |
| Synaptic adhesion-like molecules | R-HSA-8849932 | 5.308988e-01 | 0.275 | 0 | 0 |
| Serotonin Neurotransmitter Release Cycle | R-HSA-181429 | 5.308988e-01 | 0.275 | 0 | 0 |
| Protein ubiquitination | R-HSA-8852135 | 5.558143e-01 | 0.255 | 0 | 0 |
| Membrane binding and targetting of GAG proteins | R-HSA-174490 | 6.128187e-01 | 0.213 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 6.686428e-01 | 0.175 | 1 | 0 |
| Intracellular metabolism of fatty acids regulates insulin secretion | R-HSA-434313 | 6.658995e-01 | 0.177 | 0 | 0 |
| Cargo concentration in the ER | R-HSA-5694530 | 6.589744e-01 | 0.181 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 5.306403e-01 | 0.275 | 0 | 0 |
| Synthesis of PIPs at the plasma membrane | R-HSA-1660499 | 2.389914e-01 | 0.622 | 0 | 0 |
| Signaling by FGFR in disease | R-HSA-1226099 | 4.151840e-01 | 0.382 | 0 | 0 |
| Signal Transduction | R-HSA-162582 | 5.618746e-01 | 0.250 | 1 | 0 |
| Regulation of RUNX2 expression and activity | R-HSA-8939902 | 6.021027e-01 | 0.220 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 1.529716e-01 | 0.815 | 0 | 0 |
| Nervous system development | R-HSA-9675108 | 4.423536e-01 | 0.354 | 0 | 0 |
| Nuclear Events (kinase and transcription factor activation) | R-HSA-198725 | 1.841629e-01 | 0.735 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 2.853249e-01 | 0.545 | 0 | 0 |
| Signaling by FGFR4 in disease | R-HSA-5655291 | 3.751729e-01 | 0.426 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 2.360404e-01 | 0.627 | 0 | 0 |
| Axon guidance | R-HSA-422475 | 4.644546e-01 | 0.333 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 5.863767e-01 | 0.232 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 3.956394e-01 | 0.403 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 3.956394e-01 | 0.403 | 0 | 0 |
| STAT3 nuclear events downstream of ALK signaling | R-HSA-9701898 | 6.724913e-01 | 0.172 | 0 | 0 |
| Regulation of NPAS4 gene transcription | R-HSA-9768777 | 4.292122e-01 | 0.367 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 5.013632e-01 | 0.300 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 5.013632e-01 | 0.300 | 0 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 1.172576e-01 | 0.931 | 0 | 0 |
| FLT3 signaling in disease | R-HSA-9682385 | 2.729919e-01 | 0.564 | 0 | 0 |
| FLT3 Signaling | R-HSA-9607240 | 3.688397e-01 | 0.433 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 3.863206e-01 | 0.413 | 0 | 0 |
| Cilium Assembly | R-HSA-5617833 | 5.628938e-01 | 0.250 | 1 | 0 |
| Smooth Muscle Contraction | R-HSA-445355 | 6.123754e-01 | 0.213 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 6.548685e-01 | 0.184 | 0 | 0 |
| Maternal to zygotic transition (MZT) | R-HSA-9816359 | 3.160690e-01 | 0.500 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 6.132056e-01 | 0.212 | 0 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 6.132056e-01 | 0.212 | 0 | 0 |
| SARS-CoV-1 targets host intracellular signalling and regulatory pathways | R-HSA-9735871 | 4.076644e-01 | 0.390 | 0 | 0 |
| Long-term potentiation | R-HSA-9620244 | 5.215684e-01 | 0.283 | 0 | 0 |
| Ovarian tumor domain proteases | R-HSA-5689896 | 6.202740e-01 | 0.207 | 1 | 1 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 6.453878e-01 | 0.190 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 6.380325e-01 | 0.195 | 0 | 0 |
| PI Metabolism | R-HSA-1483255 | 4.041571e-01 | 0.393 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 4.495845e-01 | 0.347 | 0 | 0 |
| Signaling by KIT in disease | R-HSA-9669938 | 6.623823e-01 | 0.179 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 6.613331e-01 | 0.180 | 0 | 0 |
| MAP kinase activation | R-HSA-450294 | 6.021027e-01 | 0.220 | 0 | 0 |
| Activation of NOXA and translocation to mitochondria | R-HSA-111448 | 1.665160e-01 | 0.779 | 0 | 0 |
| Heme signaling | R-HSA-9707616 | 2.389914e-01 | 0.622 | 0 | 0 |
| Interleukin-27 signaling | R-HSA-9020956 | 4.696760e-01 | 0.328 | 0 | 0 |
| Carnitine shuttle | R-HSA-200425 | 4.702687e-01 | 0.328 | 0 | 0 |
| Regulation of CDH19 Expression and Function | R-HSA-9764302 | 6.226079e-01 | 0.206 | 0 | 0 |
| Pyrimidine salvage | R-HSA-73614 | 5.937077e-01 | 0.226 | 0 | 0 |
| Interleukin-17 signaling | R-HSA-448424 | 6.084681e-01 | 0.216 | 0 | 0 |
| Synthesis And Processing Of GAG, GAGPOL Polyproteins | R-HSA-174495 | 6.436421e-01 | 0.191 | 0 | 0 |
| Regulation of Expression and Function of Type II Classical Cadherins | R-HSA-9764260 | 1.082807e-01 | 0.965 | 0 | 0 |
| Regulation of CDH11 Expression and Function | R-HSA-9759475 | 1.395247e-01 | 0.855 | 0 | 0 |
| Interleukin-35 Signalling | R-HSA-8984722 | 5.799941e-01 | 0.237 | 0 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 5.018325e-01 | 0.299 | 0 | 0 |
| Signaling by ALK | R-HSA-201556 | 1.141788e-01 | 0.942 | 0 | 0 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | R-HSA-8866652 | 2.176397e-01 | 0.662 | 0 | 0 |
| RUNX2 regulates osteoblast differentiation | R-HSA-8940973 | 2.370448e-01 | 0.625 | 0 | 0 |
| ISG15 antiviral mechanism | R-HSA-1169408 | 1.429452e-01 | 0.845 | 0 | 0 |
| Regulation of KIT signaling | R-HSA-1433559 | 3.751729e-01 | 0.426 | 0 | 0 |
| Base Excision Repair | R-HSA-73884 | 4.304673e-01 | 0.366 | 0 | 0 |
| Activation of BH3-only proteins | R-HSA-114452 | 2.772803e-01 | 0.557 | 0 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 3.627365e-01 | 0.440 | 0 | 0 |
| Formation of the dystrophin-glycoprotein complex (DGC) | R-HSA-9913351 | 4.691085e-01 | 0.329 | 0 | 0 |
| TBC/RABGAPs | R-HSA-8854214 | 4.275539e-01 | 0.369 | 0 | 0 |
| Recycling pathway of L1 | R-HSA-437239 | 5.045504e-01 | 0.297 | 0 | 0 |
| Signaling by TGFBR3 | R-HSA-9839373 | 3.382880e-01 | 0.471 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 3.587997e-01 | 0.445 | 1 | 1 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 3.748185e-01 | 0.426 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 4.080000e-01 | 0.389 | 0 | 0 |
| Regulation of MITF-M dependent genes involved in invasion | R-HSA-9854909 | 2.101609e-01 | 0.677 | 0 | 0 |
| Depolymerization of the Nuclear Lamina | R-HSA-4419969 | 1.523316e-01 | 0.817 | 1 | 1 |
| Diseases of Mismatch Repair (MMR) | R-HSA-5423599 | 4.560986e-01 | 0.341 | 0 | 0 |
| AKT phosphorylates targets in the cytosol | R-HSA-198323 | 3.093685e-01 | 0.510 | 0 | 0 |
| SLC-mediated bile acid transport | R-HSA-9958517 | 3.871689e-01 | 0.412 | 0 | 0 |
| CLEC7A (Dectin-1) induces NFAT activation | R-HSA-5607763 | 3.751729e-01 | 0.426 | 0 | 0 |
| Retrograde neurotrophin signalling | R-HSA-177504 | 3.751729e-01 | 0.426 | 0 | 0 |
| Activation of RAC1 downstream of NMDARs | R-HSA-9619229 | 4.292122e-01 | 0.367 | 0 | 0 |
| Sensory perception of sour taste | R-HSA-9729555 | 5.184800e-01 | 0.285 | 0 | 0 |
| Pyrophosphate hydrolysis | R-HSA-71737 | 5.737099e-01 | 0.241 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 3.472958e-01 | 0.459 | 0 | 0 |
| Signalling to p38 via RIT and RIN | R-HSA-187706 | 6.226079e-01 | 0.206 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in apoptosis | R-HSA-9824594 | 6.132056e-01 | 0.212 | 0 | 0 |
| Synthesis of dolichyl-phosphate-glucose | R-HSA-480985 | 6.658995e-01 | 0.177 | 0 | 0 |
| Integration of viral DNA into host genomic DNA | R-HSA-175567 | 6.658995e-01 | 0.177 | 0 | 0 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | R-HSA-8864260 | 3.027662e-01 | 0.519 | 0 | 0 |
| TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain | R-HSA-6803205 | 2.575452e-01 | 0.589 | 0 | 0 |
| Signaling by NTRK3 (TRKC) | R-HSA-9034015 | 6.383802e-01 | 0.195 | 0 | 0 |
| RUNX2 regulates bone development | R-HSA-8941326 | 2.729919e-01 | 0.564 | 0 | 0 |
| MAPK targets/ Nuclear events mediated by MAP kinases | R-HSA-450282 | 6.162696e-01 | 0.210 | 0 | 0 |
| Nephrin family interactions | R-HSA-373753 | 1.921360e-01 | 0.716 | 0 | 0 |
| Nonhomologous End-Joining (NHEJ) | R-HSA-5693571 | 3.743801e-01 | 0.427 | 0 | 0 |
| Post NMDA receptor activation events | R-HSA-438064 | 6.200927e-01 | 0.208 | 0 | 0 |
| Apoptotic cleavage of cell adhesion proteins | R-HSA-351906 | 1.520406e-01 | 0.818 | 0 | 0 |
| Signaling by Hippo | R-HSA-2028269 | 1.338687e-01 | 0.873 | 0 | 0 |
| Uptake and function of anthrax toxins | R-HSA-5210891 | 1.338687e-01 | 0.873 | 0 | 0 |
| Signal regulatory protein family interactions | R-HSA-391160 | 3.751729e-01 | 0.426 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 1.752721e-01 | 0.756 | 0 | 0 |
| Netrin-1 signaling | R-HSA-373752 | 3.027662e-01 | 0.519 | 0 | 0 |
| NFE2L2 regulating anti-oxidant/detoxification enzymes | R-HSA-9818027 | 3.614135e-01 | 0.442 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 3.244474e-01 | 0.489 | 0 | 0 |
| tRNA processing in the nucleus | R-HSA-6784531 | 3.500751e-01 | 0.456 | 0 | 0 |
| Suppression of apoptosis | R-HSA-9635465 | 5.083696e-01 | 0.294 | 0 | 0 |
| PECAM1 interactions | R-HSA-210990 | 5.083696e-01 | 0.294 | 0 | 0 |
| Tie2 Signaling | R-HSA-210993 | 5.308988e-01 | 0.275 | 0 | 0 |
| TP53 Regulates Transcription of Death Receptors and Ligands | R-HSA-6803211 | 6.436421e-01 | 0.191 | 0 | 0 |
| Regulation of NFE2L2 gene expression | R-HSA-9818749 | 6.658995e-01 | 0.177 | 0 | 0 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | R-HSA-9705671 | 6.633613e-01 | 0.178 | 0 | 0 |
| Formation of the anterior neural plate | R-HSA-9823739 | 4.076644e-01 | 0.390 | 0 | 0 |
| Diseases of DNA repair | R-HSA-9675135 | 2.172506e-01 | 0.663 | 0 | 0 |
| TNF signaling | R-HSA-75893 | 2.578566e-01 | 0.589 | 0 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 2.790623e-01 | 0.554 | 1 | 0 |
| NrCAM interactions | R-HSA-447038 | 2.101609e-01 | 0.677 | 0 | 0 |
| Displacement of DNA glycosylase by APEX1 | R-HSA-110357 | 3.438156e-01 | 0.464 | 0 | 0 |
| Regulation of MITF-M dependent genes involved in metabolism | R-HSA-9854907 | 4.560986e-01 | 0.341 | 0 | 0 |
| Transport of Ribonucleoproteins into the Host Nucleus | R-HSA-168271 | 1.368994e-01 | 0.864 | 0 | 0 |
| Synthesis of IP3 and IP4 in the cytosol | R-HSA-1855204 | 3.401020e-01 | 0.468 | 0 | 0 |
| RUNX2 regulates chondrocyte maturation | R-HSA-8941284 | 5.737099e-01 | 0.241 | 0 | 0 |
| Regulation of TP53 Activity through Methylation | R-HSA-6804760 | 5.308988e-01 | 0.275 | 0 | 0 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | R-HSA-9617324 | 6.383802e-01 | 0.195 | 0 | 0 |
| CREB phosphorylation | R-HSA-199920 | 6.658995e-01 | 0.177 | 0 | 0 |
| NADPH regeneration | R-HSA-389542 | 6.658995e-01 | 0.177 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 4.971095e-01 | 0.304 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 4.971095e-01 | 0.304 | 0 | 0 |
| Inositol phosphate metabolism | R-HSA-1483249 | 4.422476e-01 | 0.354 | 0 | 0 |
| Transcriptional Regulation by NPAS4 | R-HSA-9634815 | 4.469719e-01 | 0.350 | 0 | 0 |
| ChREBP activates metabolic gene expression | R-HSA-163765 | 2.440368e-01 | 0.613 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 4.911417e-01 | 0.309 | 0 | 0 |
| Biotin transport and metabolism | R-HSA-196780 | 6.724913e-01 | 0.172 | 0 | 0 |
| RMTs methylate histone arginines | R-HSA-3214858 | 4.470283e-01 | 0.350 | 0 | 0 |
| Maturation of nucleoprotein | R-HSA-9683610 | 3.423366e-01 | 0.466 | 0 | 0 |
| YAP1- and WWTR1 (TAZ)-stimulated gene expression | R-HSA-2032785 | 3.751729e-01 | 0.426 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 2.432568e-01 | 0.614 | 0 | 0 |
| Collagen chain trimerization | R-HSA-8948216 | 6.202740e-01 | 0.207 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in DNA replication, damage repair and senescence | R-HSA-9825895 | 3.871689e-01 | 0.412 | 0 | 0 |
| Export of Viral Ribonucleoproteins from Nucleus | R-HSA-168274 | 2.172506e-01 | 0.663 | 0 | 0 |
| Release of Hh-Np from the secreting cell | R-HSA-5362798 | 6.226079e-01 | 0.206 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | R-HSA-9825892 | 6.383802e-01 | 0.195 | 0 | 0 |
| Mitochondrial calcium ion transport | R-HSA-8949215 | 6.383802e-01 | 0.195 | 0 | 0 |
| HDL clearance | R-HSA-8964011 | 6.658995e-01 | 0.177 | 0 | 0 |
| Regulation of TNFR1 signaling | R-HSA-5357905 | 3.382880e-01 | 0.471 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 2.165862e-01 | 0.664 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 3.336170e-01 | 0.477 | 0 | 0 |
| Growth hormone receptor signaling | R-HSA-982772 | 4.702687e-01 | 0.328 | 0 | 0 |
| Interleukin-15 signaling | R-HSA-8983432 | 3.093685e-01 | 0.510 | 0 | 0 |
| Intrinsic Pathway for Apoptosis | R-HSA-109606 | 6.612600e-01 | 0.180 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 3.493313e-01 | 0.457 | 0 | 0 |
| NS1 Mediated Effects on Host Pathways | R-HSA-168276 | 1.141788e-01 | 0.942 | 0 | 0 |
| Physiological factors | R-HSA-5578768 | 3.751729e-01 | 0.426 | 0 | 0 |
| Receptor-type tyrosine-protein phosphatases | R-HSA-388844 | 4.396269e-01 | 0.357 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | R-HSA-6803204 | 5.703763e-01 | 0.244 | 0 | 0 |
| PTK6 Regulates Proteins Involved in RNA Processing | R-HSA-8849468 | 5.737099e-01 | 0.241 | 0 | 0 |
| Maturation of nucleoprotein | R-HSA-9694631 | 5.594251e-01 | 0.252 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in extracellular matrix, focal adhesion and epithelial-to-mesenchymal transition | R-HSA-9926550 | 5.308988e-01 | 0.275 | 0 | 0 |
| OAS antiviral response | R-HSA-8983711 | 5.799941e-01 | 0.237 | 0 | 0 |
| XBP1(S) activates chaperone genes | R-HSA-381038 | 4.885295e-01 | 0.311 | 0 | 0 |
| Nectin/Necl trans heterodimerization | R-HSA-420597 | 5.737099e-01 | 0.241 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 6.612600e-01 | 0.180 | 0 | 0 |
| Zygotic genome activation (ZGA) | R-HSA-9819196 | 3.899877e-01 | 0.409 | 0 | 0 |
| Interleukin-7 signaling | R-HSA-1266695 | 5.215684e-01 | 0.283 | 0 | 0 |
| IRE1alpha activates chaperones | R-HSA-381070 | 5.726637e-01 | 0.242 | 0 | 0 |
| Signaling by Leptin | R-HSA-2586552 | 4.696760e-01 | 0.328 | 0 | 0 |
| Maturation of hRSV A proteins | R-HSA-9828806 | 5.703763e-01 | 0.244 | 0 | 0 |
| Translation of Replicase and Assembly of the Replication Transcription Complex | R-HSA-9679504 | 5.308988e-01 | 0.275 | 0 | 0 |
| Translation of Replicase and Assembly of the Replication Transcription Complex | R-HSA-9694676 | 6.623823e-01 | 0.179 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 6.742155e-01 | 0.171 | 0 | 0 |
| Attenuation phase | R-HSA-3371568 | 6.766130e-01 | 0.170 | 0 | 0 |
| Aggrephagy | R-HSA-9646399 | 6.766130e-01 | 0.170 | 0 | 0 |
| Transcriptional regulation of brown and beige adipocyte differentiation by EBF2 | R-HSA-9844594 | 6.766130e-01 | 0.170 | 0 | 0 |
| Transcriptional regulation of brown and beige adipocyte differentiation | R-HSA-9843743 | 6.766130e-01 | 0.170 | 0 | 0 |
| Nuclear signaling by ERBB4 | R-HSA-1251985 | 6.766130e-01 | 0.170 | 0 | 0 |
| Regulation of PD-L1(CD274) transcription | R-HSA-9909649 | 6.780026e-01 | 0.169 | 0 | 0 |
| Downregulation of SMAD2/3:SMAD4 transcriptional activity | R-HSA-2173795 | 6.790809e-01 | 0.168 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 6.797655e-01 | 0.168 | 0 | 0 |
| Gene Silencing by RNA | R-HSA-211000 | 6.889997e-01 | 0.162 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 6.898867e-01 | 0.161 | 0 | 0 |
| Toll Like Receptor 9 (TLR9) Cascade | R-HSA-168138 | 6.915534e-01 | 0.160 | 0 | 0 |
| Meiosis | R-HSA-1500620 | 6.944225e-01 | 0.158 | 0 | 0 |
| Assembly of the ORC complex at the origin of replication | R-HSA-68616 | 6.983439e-01 | 0.156 | 0 | 0 |
| Negative regulation of FGFR1 signaling | R-HSA-5654726 | 6.983439e-01 | 0.156 | 0 | 0 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | R-HSA-442742 | 6.983439e-01 | 0.156 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 6.990607e-01 | 0.155 | 0 | 0 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | R-HSA-399955 | 6.994137e-01 | 0.155 | 0 | 0 |
| Regulation of BACH1 activity | R-HSA-9708530 | 6.994137e-01 | 0.155 | 0 | 0 |
| Regulation of NF-kappa B signaling | R-HSA-9758274 | 6.994137e-01 | 0.155 | 0 | 0 |
| Negative regulation of FLT3 | R-HSA-9706369 | 6.994137e-01 | 0.155 | 0 | 0 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | R-HSA-210744 | 6.994137e-01 | 0.155 | 0 | 0 |
| Activation of SMO | R-HSA-5635838 | 6.994137e-01 | 0.155 | 0 | 0 |
| Induction of Cell-Cell Fusion | R-HSA-9733458 | 6.994137e-01 | 0.155 | 0 | 0 |
| MET activates PI3K/AKT signaling | R-HSA-8851907 | 7.042272e-01 | 0.152 | 0 | 0 |
| RUNX3 Regulates Immune Response and Cell Migration | R-HSA-8949275 | 7.042272e-01 | 0.152 | 0 | 0 |
| Disinhibition of SNARE formation | R-HSA-114516 | 7.042272e-01 | 0.152 | 0 | 0 |
| Pre-NOTCH Processing in the Endoplasmic Reticulum | R-HSA-1912399 | 7.042272e-01 | 0.152 | 0 | 0 |
| SLBP independent Processing of Histone Pre-mRNAs | R-HSA-111367 | 7.042272e-01 | 0.152 | 0 | 0 |
| RUNX1 regulates estrogen receptor mediated transcription | R-HSA-8931987 | 7.042272e-01 | 0.152 | 0 | 0 |
| POU5F1 (OCT4), SOX2, NANOG repress genes related to differentiation | R-HSA-2892245 | 7.042272e-01 | 0.152 | 0 | 0 |
| Activated NTRK2 signals through CDK5 | R-HSA-9032845 | 7.042272e-01 | 0.152 | 0 | 0 |
| DAG1 core M1 glycosylations | R-HSA-8932506 | 7.042272e-01 | 0.152 | 0 | 0 |
| VLDL clearance | R-HSA-8964046 | 7.042272e-01 | 0.152 | 0 | 0 |
| Synthesis of PIPs in the nucleus | R-HSA-8847453 | 7.042272e-01 | 0.152 | 0 | 0 |
| Defective HLCS causes multiple carboxylase deficiency | R-HSA-3371599 | 7.042272e-01 | 0.152 | 0 | 0 |
| Netrin mediated repulsion signals | R-HSA-418886 | 7.042272e-01 | 0.152 | 0 | 0 |
| Regulation of PTEN localization | R-HSA-8948747 | 7.042272e-01 | 0.152 | 0 | 0 |
| Uptake and function of diphtheria toxin | R-HSA-5336415 | 7.042272e-01 | 0.152 | 0 | 0 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | R-HSA-3371497 | 7.057183e-01 | 0.151 | 0 | 0 |
| PTEN Regulation | R-HSA-6807070 | 7.088975e-01 | 0.149 | 0 | 0 |
| Intra-Golgi traffic | R-HSA-6811438 | 7.109278e-01 | 0.148 | 0 | 0 |
| Miscellaneous transport and binding events | R-HSA-5223345 | 7.167614e-01 | 0.145 | 0 | 0 |
| Activation of NMDA receptors and postsynaptic events | R-HSA-442755 | 7.201444e-01 | 0.143 | 0 | 0 |
| Mitochondrial biogenesis | R-HSA-1592230 | 7.226368e-01 | 0.141 | 0 | 0 |
| mRNA decay by 5' to 3' exoribonuclease | R-HSA-430039 | 7.244716e-01 | 0.140 | 0 | 0 |
| Activation of IRF3, IRF7 mediated by TBK1, IKKε (IKBKE) | R-HSA-936964 | 7.244716e-01 | 0.140 | 0 | 0 |
| TRAF3-dependent IRF activation pathway | R-HSA-918233 | 7.244716e-01 | 0.140 | 0 | 0 |
| Fibronectin matrix formation | R-HSA-1566977 | 7.244716e-01 | 0.140 | 0 | 0 |
| Acyl chain remodelling of PS | R-HSA-1482801 | 7.273430e-01 | 0.138 | 0 | 0 |
| Negative regulation of FGFR2 signaling | R-HSA-5654727 | 7.343365e-01 | 0.134 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | R-HSA-110328 | 7.343365e-01 | 0.134 | 0 | 0 |
| NPAS4 regulates expression of target genes | R-HSA-9768919 | 7.343365e-01 | 0.134 | 0 | 0 |
| RNA Polymerase I Promoter Escape | R-HSA-73772 | 7.372408e-01 | 0.132 | 0 | 0 |
| Orc1 removal from chromatin | R-HSA-68949 | 7.372408e-01 | 0.132 | 0 | 0 |
| Uptake and actions of bacterial toxins | R-HSA-5339562 | 7.372408e-01 | 0.132 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of myeloid cells | R-HSA-8939246 | 7.381600e-01 | 0.132 | 0 | 0 |
| Activated NTRK2 signals through PI3K | R-HSA-9028335 | 7.381600e-01 | 0.132 | 0 | 0 |
| MET receptor recycling | R-HSA-8875656 | 7.381600e-01 | 0.132 | 0 | 0 |
| Myoclonic epilepsy of Lafora | R-HSA-3785653 | 7.381600e-01 | 0.132 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of keratinocytes | R-HSA-8939242 | 7.381600e-01 | 0.132 | 0 | 0 |
| Nef mediated downregulation of MHC class I complex cell surface expression | R-HSA-164940 | 7.381600e-01 | 0.132 | 0 | 0 |
| Interleukin-23 signaling | R-HSA-9020933 | 7.381600e-01 | 0.132 | 0 | 0 |
| Adrenoceptors | R-HSA-390696 | 7.381600e-01 | 0.132 | 0 | 0 |
| Negative regulation of activity of TFAP2 (AP-2) family transcription factors | R-HSA-8866904 | 7.381600e-01 | 0.132 | 0 | 0 |
| Co-stimulation by ICOS | R-HSA-9927354 | 7.381600e-01 | 0.132 | 0 | 0 |
| BH3-only proteins associate with and inactivate anti-apoptotic BCL-2 members | R-HSA-111453 | 7.381600e-01 | 0.132 | 0 | 0 |
| DAG1 core M2 glycosylations | R-HSA-8932504 | 7.381600e-01 | 0.132 | 0 | 0 |
| PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 | R-HSA-8849469 | 7.381600e-01 | 0.132 | 0 | 0 |
| Downregulation of ERBB4 signaling | R-HSA-1253288 | 7.381600e-01 | 0.132 | 0 | 0 |
| Activated NTRK2 signals through FYN | R-HSA-9032500 | 7.381600e-01 | 0.132 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 7.412499e-01 | 0.130 | 0 | 0 |
| Defective pyroptosis | R-HSA-9710421 | 7.425942e-01 | 0.129 | 0 | 0 |
| Myogenesis | R-HSA-525793 | 7.466903e-01 | 0.127 | 0 | 0 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 7.466903e-01 | 0.127 | 0 | 0 |
| Removal of the Flap Intermediate from the C-strand | R-HSA-174437 | 7.477383e-01 | 0.126 | 0 | 0 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | R-HSA-164938 | 7.477383e-01 | 0.126 | 0 | 0 |
| Elevation of cytosolic Ca2+ levels | R-HSA-139853 | 7.477383e-01 | 0.126 | 0 | 0 |
| Specification of primordial germ cells | R-HSA-9827857 | 7.477383e-01 | 0.126 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 7.478867e-01 | 0.126 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 7.513928e-01 | 0.124 | 0 | 0 |
| Transcriptional regulation of white adipocyte differentiation | R-HSA-381340 | 7.517726e-01 | 0.124 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 7.574377e-01 | 0.121 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 7.609264e-01 | 0.119 | 0 | 0 |
| Toll Like Receptor 3 (TLR3) Cascade | R-HSA-168164 | 7.612764e-01 | 0.118 | 0 | 0 |
| Processive synthesis on the C-strand of the telomere | R-HSA-174414 | 7.649233e-01 | 0.116 | 0 | 0 |
| Tat-mediated HIV elongation arrest and recovery | R-HSA-167243 | 7.649233e-01 | 0.116 | 0 | 0 |
| Pausing and recovery of Tat-mediated HIV elongation | R-HSA-167238 | 7.649233e-01 | 0.116 | 0 | 0 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | R-HSA-4641262 | 7.649233e-01 | 0.116 | 0 | 0 |
| Signaling by FGFR3 in disease | R-HSA-5655332 | 7.649233e-01 | 0.116 | 0 | 0 |
| CD28 dependent PI3K/Akt signaling | R-HSA-389357 | 7.649233e-01 | 0.116 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 7.669945e-01 | 0.115 | 0 | 0 |
| Regulation of TP53 Degradation | R-HSA-6804757 | 7.669945e-01 | 0.115 | 1 | 1 |
| MASTL Facilitates Mitotic Progression | R-HSA-2465910 | 7.682016e-01 | 0.115 | 1 | 1 |
| AMPK inhibits chREBP transcriptional activation activity | R-HSA-163680 | 7.682016e-01 | 0.115 | 0 | 0 |
| Inactivation of CDC42 and RAC1 | R-HSA-428543 | 7.682016e-01 | 0.115 | 0 | 0 |
| Unwinding of DNA | R-HSA-176974 | 7.682016e-01 | 0.115 | 0 | 0 |
| Activation of the AP-1 family of transcription factors | R-HSA-450341 | 7.682016e-01 | 0.115 | 0 | 0 |
| NOTCH4 Activation and Transmission of Signal to the Nucleus | R-HSA-9013700 | 7.682016e-01 | 0.115 | 0 | 0 |
| mRNA Editing | R-HSA-75072 | 7.682016e-01 | 0.115 | 0 | 0 |
| ARMS-mediated activation | R-HSA-170984 | 7.682016e-01 | 0.115 | 0 | 0 |
| Regulation of signaling by NODAL | R-HSA-1433617 | 7.682016e-01 | 0.115 | 0 | 0 |
| WNT mediated activation of DVL | R-HSA-201688 | 7.682016e-01 | 0.115 | 0 | 0 |
| Regulation of commissural axon pathfinding by SLIT and ROBO | R-HSA-428542 | 7.682016e-01 | 0.115 | 0 | 0 |
| Regulated proteolysis of p75NTR | R-HSA-193692 | 7.682016e-01 | 0.115 | 0 | 0 |
| Lipophagy | R-HSA-9613354 | 7.682016e-01 | 0.115 | 0 | 0 |
| Zinc influx into cells by the SLC39 gene family | R-HSA-442380 | 7.682016e-01 | 0.115 | 0 | 0 |
| Defects in biotin (Btn) metabolism | R-HSA-3323169 | 7.682016e-01 | 0.115 | 0 | 0 |
| Cellular response to mitochondrial stress | R-HSA-9840373 | 7.682016e-01 | 0.115 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 7.686775e-01 | 0.114 | 0 | 0 |
| RNA Polymerase III Transcription Termination | R-HSA-73980 | 7.692951e-01 | 0.114 | 0 | 0 |
| PKA activation in glucagon signalling | R-HSA-164378 | 7.692951e-01 | 0.114 | 0 | 0 |
| PKA activation | R-HSA-163615 | 7.692951e-01 | 0.114 | 0 | 0 |
| Nephron development | R-HSA-9831926 | 7.692951e-01 | 0.114 | 0 | 0 |
| MyD88 cascade initiated on plasma membrane | R-HSA-975871 | 7.719846e-01 | 0.112 | 0 | 0 |
| Toll Like Receptor 5 (TLR5) Cascade | R-HSA-168176 | 7.719846e-01 | 0.112 | 0 | 0 |
| Toll Like Receptor 10 (TLR10) Cascade | R-HSA-168142 | 7.719846e-01 | 0.112 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 7.786317e-01 | 0.109 | 0 | 0 |
| Formation of the HIV-1 Early Elongation Complex | R-HSA-167158 | 7.820736e-01 | 0.107 | 0 | 0 |
| HIV elongation arrest and recovery | R-HSA-167287 | 7.820736e-01 | 0.107 | 0 | 0 |
| Activation of AMPK downstream of NMDARs | R-HSA-9619483 | 7.820736e-01 | 0.107 | 0 | 0 |
| Formation of the Early Elongation Complex | R-HSA-113418 | 7.820736e-01 | 0.107 | 0 | 0 |
| Pausing and recovery of HIV elongation | R-HSA-167290 | 7.820736e-01 | 0.107 | 0 | 0 |
| Activation of kainate receptors upon glutamate binding | R-HSA-451326 | 7.820736e-01 | 0.107 | 0 | 0 |
| Voltage gated Potassium channels | R-HSA-1296072 | 7.821044e-01 | 0.107 | 0 | 0 |
| Adipogenesis | R-HSA-9843745 | 7.865956e-01 | 0.104 | 0 | 0 |
| Host Interactions of HIV factors | R-HSA-162909 | 7.871489e-01 | 0.104 | 0 | 0 |
| PI-3K cascade:FGFR3 | R-HSA-5654710 | 7.892278e-01 | 0.103 | 0 | 0 |
| Abortive elongation of HIV-1 transcript in the absence of Tat | R-HSA-167242 | 7.892278e-01 | 0.103 | 0 | 0 |
| Germ layer formation at gastrulation | R-HSA-9754189 | 7.892278e-01 | 0.103 | 0 | 0 |
| Other interleukin signaling | R-HSA-449836 | 7.892278e-01 | 0.103 | 0 | 0 |
| Mechanical load activates signaling by PIEZO1 and integrins in osteocytes | R-HSA-9856532 | 7.892278e-01 | 0.103 | 0 | 0 |
| Signaling by FGFR1 | R-HSA-5654736 | 7.896892e-01 | 0.103 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 7.933393e-01 | 0.101 | 0 | 0 |
| Signaling by Insulin receptor | R-HSA-74752 | 7.933393e-01 | 0.101 | 0 | 0 |
| Regulation of lipid metabolism by PPARalpha | R-HSA-400206 | 7.937981e-01 | 0.100 | 0 | 0 |
| Erythropoietin activates Phospholipase C gamma (PLCG) | R-HSA-9027277 | 7.947980e-01 | 0.100 | 0 | 0 |
| Folding of actin by CCT/TriC | R-HSA-390450 | 7.947980e-01 | 0.100 | 0 | 0 |
| TET1,2,3 and TDG demethylate DNA | R-HSA-5221030 | 7.947980e-01 | 0.100 | 0 | 0 |
| Josephin domain DUBs | R-HSA-5689877 | 7.947980e-01 | 0.100 | 0 | 0 |
| Ion influx/efflux at host-pathogen interface | R-HSA-6803544 | 7.947980e-01 | 0.100 | 0 | 0 |
| Formation of intermediate mesoderm | R-HSA-9761174 | 7.947980e-01 | 0.100 | 0 | 0 |
| EGFR Transactivation by Gastrin | R-HSA-2179392 | 7.947980e-01 | 0.100 | 0 | 0 |
| Arachidonate production from DAG | R-HSA-426048 | 7.947980e-01 | 0.100 | 0 | 0 |
| Cross-presentation of particulate exogenous antigens (phagosomes) | R-HSA-1236973 | 7.947980e-01 | 0.100 | 0 | 0 |
| Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RNA | R-HSA-428359 | 7.947980e-01 | 0.100 | 0 | 0 |
| 2-LTR circle formation | R-HSA-164843 | 7.947980e-01 | 0.100 | 0 | 0 |
| Sperm Motility And Taxes | R-HSA-1300642 | 7.947980e-01 | 0.100 | 0 | 0 |
| Formation of apoptosome | R-HSA-111458 | 7.947980e-01 | 0.100 | 0 | 0 |
| Regulation of the apoptosome activity | R-HSA-9627069 | 7.947980e-01 | 0.100 | 0 | 0 |
| Regulation of CDH11 function | R-HSA-9762292 | 7.947980e-01 | 0.100 | 0 | 0 |
| DNA methylation | R-HSA-5334118 | 7.981767e-01 | 0.098 | 0 | 0 |
| Endosomal Sorting Complex Required For Transport (ESCRT) | R-HSA-917729 | 7.981767e-01 | 0.098 | 0 | 0 |
| Downstream signaling of activated FGFR3 | R-HSA-5654708 | 7.981767e-01 | 0.098 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 7.981767e-01 | 0.098 | 0 | 0 |
| DARPP-32 events | R-HSA-180024 | 7.981767e-01 | 0.098 | 0 | 0 |
| UCH proteinases | R-HSA-5689603 | 8.004450e-01 | 0.097 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 8.051744e-01 | 0.094 | 0 | 0 |
| TRIF (TICAM1)-mediated TLR4 signaling | R-HSA-937061 | 8.065956e-01 | 0.093 | 0 | 0 |
| MyD88-independent TLR4 cascade | R-HSA-166166 | 8.065956e-01 | 0.093 | 0 | 0 |
| Regulation of PD-L1(CD274) translation | R-HSA-9909620 | 8.076254e-01 | 0.093 | 0 | 0 |
| PI-3K cascade:FGFR4 | R-HSA-5654720 | 8.076254e-01 | 0.093 | 0 | 0 |
| BBSome-mediated cargo-targeting to cilium | R-HSA-5620922 | 8.076254e-01 | 0.093 | 0 | 0 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | R-HSA-167200 | 8.099761e-01 | 0.092 | 0 | 0 |
| Regulation of TP53 Expression and Degradation | R-HSA-6806003 | 8.099761e-01 | 0.092 | 1 | 0 |
| Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian Skin | R-HSA-9725554 | 8.099761e-01 | 0.092 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 8.099761e-01 | 0.092 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 8.103892e-01 | 0.091 | 0 | 0 |
| Metal ion SLC transporters | R-HSA-425410 | 8.103892e-01 | 0.091 | 0 | 0 |
| Collagen formation | R-HSA-1474290 | 8.117676e-01 | 0.091 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 8.117676e-01 | 0.091 | 0 | 0 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | R-HSA-72662 | 8.127277e-01 | 0.090 | 0 | 0 |
| NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux | R-HSA-9029569 | 8.127277e-01 | 0.090 | 0 | 0 |
| Downstream signaling of activated FGFR4 | R-HSA-5654716 | 8.132709e-01 | 0.090 | 0 | 0 |
| Interleukin-37 signaling | R-HSA-9008059 | 8.132709e-01 | 0.090 | 0 | 0 |
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | R-HSA-933543 | 8.183441e-01 | 0.087 | 0 | 0 |
| Signaling by APC mutants | R-HSA-4839744 | 8.183441e-01 | 0.087 | 0 | 0 |
| AXIN missense mutants destabilize the destruction complex | R-HSA-5467340 | 8.183441e-01 | 0.087 | 0 | 0 |
| APC truncation mutants have impaired AXIN binding | R-HSA-5467337 | 8.183441e-01 | 0.087 | 0 | 0 |
| Truncations of AMER1 destabilize the destruction complex | R-HSA-5467348 | 8.183441e-01 | 0.087 | 0 | 0 |
| LGI-ADAM interactions | R-HSA-5682910 | 8.183441e-01 | 0.087 | 0 | 0 |
| Activated NTRK3 signals through RAS | R-HSA-9034864 | 8.183441e-01 | 0.087 | 0 | 0 |
| InlA-mediated entry of Listeria monocytogenes into host cells | R-HSA-8876493 | 8.183441e-01 | 0.087 | 0 | 0 |
| RHOBTB3 ATPase cycle | R-HSA-9706019 | 8.183441e-01 | 0.087 | 0 | 0 |
| DAG1 core M3 glycosylations | R-HSA-8932505 | 8.183441e-01 | 0.087 | 0 | 0 |
| Inorganic anion exchange by SLC26 transporters | R-HSA-427601 | 8.183441e-01 | 0.087 | 0 | 0 |
| SARS-CoV-2 modulates autophagy | R-HSA-9754560 | 8.183441e-01 | 0.087 | 0 | 0 |
| Chylomicron assembly | R-HSA-8963888 | 8.183441e-01 | 0.087 | 0 | 0 |
| Interleukin-2 signaling | R-HSA-9020558 | 8.183441e-01 | 0.087 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 8.216352e-01 | 0.085 | 0 | 0 |
| p53-Dependent G1 DNA Damage Response | R-HSA-69563 | 8.220805e-01 | 0.085 | 0 | 0 |
| p53-Dependent G1/S DNA damage checkpoint | R-HSA-69580 | 8.220805e-01 | 0.085 | 0 | 0 |
| Gap junction trafficking and regulation | R-HSA-157858 | 8.220805e-01 | 0.085 | 0 | 0 |
| Inhibition of DNA recombination at telomere | R-HSA-9670095 | 8.227811e-01 | 0.085 | 0 | 0 |
| Formation of HIV elongation complex in the absence of HIV Tat | R-HSA-167152 | 8.227811e-01 | 0.085 | 0 | 0 |
| HIV Transcription Elongation | R-HSA-167169 | 8.227811e-01 | 0.085 | 0 | 0 |
| Tat-mediated elongation of the HIV-1 transcript | R-HSA-167246 | 8.227811e-01 | 0.085 | 0 | 0 |
| Extension of Telomeres | R-HSA-180786 | 8.234802e-01 | 0.084 | 0 | 0 |
| JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | R-HSA-450321 | 8.245776e-01 | 0.084 | 0 | 0 |
| NOTCH2 Activation and Transmission of Signal to the Nucleus | R-HSA-2979096 | 8.245776e-01 | 0.084 | 0 | 0 |
| PKA-mediated phosphorylation of CREB | R-HSA-111931 | 8.245776e-01 | 0.084 | 0 | 0 |
| Acetylcholine Neurotransmitter Release Cycle | R-HSA-264642 | 8.245776e-01 | 0.084 | 0 | 0 |
| ERK/MAPK targets | R-HSA-198753 | 8.245776e-01 | 0.084 | 0 | 0 |
| Early Phase of HIV Life Cycle | R-HSA-162594 | 8.245776e-01 | 0.084 | 0 | 0 |
| Basigin interactions | R-HSA-210991 | 8.245776e-01 | 0.084 | 0 | 0 |
| Trafficking of AMPA receptors | R-HSA-399719 | 8.273970e-01 | 0.082 | 0 | 0 |
| Toll Like Receptor 7/8 (TLR7/8) Cascade | R-HSA-168181 | 8.305770e-01 | 0.081 | 0 | 0 |
| Chromatin modifications during the maternal to zygotic transition (MZT) | R-HSA-9821002 | 8.348641e-01 | 0.078 | 0 | 0 |
| Signaling by FGFR2 | R-HSA-5654738 | 8.382670e-01 | 0.077 | 0 | 0 |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | R-HSA-9856530 | 8.382670e-01 | 0.077 | 0 | 0 |
| PKR-mediated signaling | R-HSA-9833482 | 8.382670e-01 | 0.077 | 1 | 1 |
| ATF6 (ATF6-alpha) activates chaperone genes | R-HSA-381183 | 8.391897e-01 | 0.076 | 0 | 0 |
| Synthesis of diphthamide-EEF2 | R-HSA-5358493 | 8.391897e-01 | 0.076 | 0 | 0 |
| Signaling by GSK3beta mutants | R-HSA-5339716 | 8.391897e-01 | 0.076 | 0 | 0 |
| Integration of provirus | R-HSA-162592 | 8.391897e-01 | 0.076 | 0 | 0 |
| Activated NTRK2 signals through RAS | R-HSA-9026519 | 8.391897e-01 | 0.076 | 0 | 0 |
| NF-kB is activated and signals survival | R-HSA-209560 | 8.391897e-01 | 0.076 | 0 | 0 |
| ERKs are inactivated | R-HSA-202670 | 8.391897e-01 | 0.076 | 0 | 0 |
| Signaling by AMER1 mutants | R-HSA-4839748 | 8.391897e-01 | 0.076 | 0 | 0 |
| Signaling by AXIN mutants | R-HSA-4839735 | 8.391897e-01 | 0.076 | 0 | 0 |
| Sensing of DNA Double Strand Breaks | R-HSA-5693548 | 8.391897e-01 | 0.076 | 0 | 0 |
| NR1H2 & NR1H3 regulate gene expression to control bile acid homeostasis | R-HSA-9623433 | 8.391897e-01 | 0.076 | 0 | 0 |
| APOBEC3G mediated resistance to HIV-1 infection | R-HSA-180689 | 8.391897e-01 | 0.076 | 0 | 0 |
| Proton-coupled monocarboxylate transport | R-HSA-433692 | 8.391897e-01 | 0.076 | 0 | 0 |
| Cytochrome c-mediated apoptotic response | R-HSA-111461 | 8.391897e-01 | 0.076 | 0 | 0 |
| FRS-mediated FGFR3 signaling | R-HSA-5654706 | 8.401738e-01 | 0.076 | 0 | 0 |
| Assembly Of The HIV Virion | R-HSA-175474 | 8.401738e-01 | 0.076 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 8.403150e-01 | 0.076 | 0 | 0 |
| Signaling by WNT in cancer | R-HSA-4791275 | 8.405970e-01 | 0.075 | 0 | 0 |
| PPARA activates gene expression | R-HSA-1989781 | 8.419565e-01 | 0.075 | 0 | 0 |
| Collagen degradation | R-HSA-1442490 | 8.435078e-01 | 0.074 | 0 | 0 |
| Assembly and cell surface presentation of NMDA receptors | R-HSA-9609736 | 8.462504e-01 | 0.073 | 0 | 0 |
| Glutamate binding, activation of AMPA receptors and synaptic plasticity | R-HSA-399721 | 8.529140e-01 | 0.069 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 8.529140e-01 | 0.069 | 0 | 0 |
| PI-3K cascade:FGFR1 | R-HSA-5654689 | 8.545019e-01 | 0.068 | 0 | 0 |
| FGFR2 alternative splicing | R-HSA-6803529 | 8.545019e-01 | 0.068 | 0 | 0 |
| Developmental Lineage of Mammary Stem Cells | R-HSA-9938206 | 8.545019e-01 | 0.068 | 0 | 0 |
| Regulation of IFNA/IFNB signaling | R-HSA-912694 | 8.545019e-01 | 0.068 | 0 | 0 |
| FRS-mediated FGFR4 signaling | R-HSA-5654712 | 8.545019e-01 | 0.068 | 0 | 0 |
| Toll Like Receptor 4 (TLR4) Cascade | R-HSA-166016 | 8.556264e-01 | 0.068 | 0 | 0 |
| Cleavage of the damaged pyrimidine | R-HSA-110329 | 8.569665e-01 | 0.067 | 0 | 0 |
| Depyrimidination | R-HSA-73928 | 8.569665e-01 | 0.067 | 0 | 0 |
| NOTCH2 intracellular domain regulates transcription | R-HSA-2197563 | 8.576442e-01 | 0.067 | 0 | 0 |
| IRAK1 recruits IKK complex upon TLR7/8 or 9 stimulation | R-HSA-975144 | 8.576442e-01 | 0.067 | 0 | 0 |
| IRAK1 recruits IKK complex | R-HSA-937039 | 8.576442e-01 | 0.067 | 0 | 0 |
| Signaling by CTNNB1 phospho-site mutants | R-HSA-4839743 | 8.576442e-01 | 0.067 | 0 | 0 |
| GRB2 events in EGFR signaling | R-HSA-179812 | 8.576442e-01 | 0.067 | 0 | 0 |
| CTNNB1 T41 mutants aren't phosphorylated | R-HSA-5358752 | 8.576442e-01 | 0.067 | 0 | 0 |
| CTNNB1 S45 mutants aren't phosphorylated | R-HSA-5358751 | 8.576442e-01 | 0.067 | 0 | 0 |
| CTNNB1 S37 mutants aren't phosphorylated | R-HSA-5358749 | 8.576442e-01 | 0.067 | 0 | 0 |
| CTNNB1 S33 mutants aren't phosphorylated | R-HSA-5358747 | 8.576442e-01 | 0.067 | 0 | 0 |
| Beta oxidation of myristoyl-CoA to lauroyl-CoA | R-HSA-77285 | 8.576442e-01 | 0.067 | 0 | 0 |
| Beta oxidation of palmitoyl-CoA to myristoyl-CoA | R-HSA-77305 | 8.576442e-01 | 0.067 | 0 | 0 |
| Serotonin clearance from the synaptic cleft | R-HSA-380615 | 8.576442e-01 | 0.067 | 0 | 0 |
| SHC-related events triggered by IGF1R | R-HSA-2428933 | 8.576442e-01 | 0.067 | 0 | 0 |
| Downregulation of ERBB2:ERBB3 signaling | R-HSA-1358803 | 8.576442e-01 | 0.067 | 0 | 0 |
| Advanced glycosylation endproduct receptor signaling | R-HSA-879415 | 8.576442e-01 | 0.067 | 0 | 0 |
| Regulation of IFNG signaling | R-HSA-877312 | 8.576442e-01 | 0.067 | 0 | 0 |
| Reversal of alkylation damage by DNA dioxygenases | R-HSA-73943 | 8.576442e-01 | 0.067 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 8.616499e-01 | 0.065 | 0 | 0 |
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | R-HSA-975138 | 8.624524e-01 | 0.064 | 0 | 0 |
| Golgi Associated Vesicle Biogenesis | R-HSA-432722 | 8.631264e-01 | 0.064 | 0 | 0 |
| Association of TriC/CCT with target proteins during biosynthesis | R-HSA-390471 | 8.643915e-01 | 0.063 | 0 | 0 |
| Glycolysis | R-HSA-70171 | 8.665862e-01 | 0.062 | 0 | 0 |
| Regulation of PTEN mRNA translation | R-HSA-8943723 | 8.676475e-01 | 0.062 | 0 | 0 |
| The role of Nef in HIV-1 replication and disease pathogenesis | R-HSA-164952 | 8.676475e-01 | 0.062 | 0 | 0 |
| Syndecan interactions | R-HSA-3000170 | 8.676475e-01 | 0.062 | 0 | 0 |
| Class I MHC mediated antigen processing & presentation | R-HSA-983169 | 8.682753e-01 | 0.061 | 0 | 0 |
| MyD88 dependent cascade initiated on endosome | R-HSA-975155 | 8.690311e-01 | 0.061 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 8.701986e-01 | 0.060 | 0 | 0 |
| Translation initiation complex formation | R-HSA-72649 | 8.720482e-01 | 0.059 | 0 | 0 |
| ATF6 (ATF6-alpha) activates chaperones | R-HSA-381033 | 8.739818e-01 | 0.058 | 0 | 0 |
| Adenylate cyclase activating pathway | R-HSA-170660 | 8.739818e-01 | 0.058 | 0 | 0 |
| Platelet Adhesion to exposed collagen | R-HSA-75892 | 8.739818e-01 | 0.058 | 0 | 0 |
| Chylomicron remodeling | R-HSA-8963901 | 8.739818e-01 | 0.058 | 0 | 0 |
| Formation of axial mesoderm | R-HSA-9796292 | 8.739818e-01 | 0.058 | 0 | 0 |
| PI5P Regulates TP53 Acetylation | R-HSA-6811555 | 8.739818e-01 | 0.058 | 0 | 0 |
| CREB1 phosphorylation through the activation of Adenylate Cyclase | R-HSA-442720 | 8.739818e-01 | 0.058 | 0 | 0 |
| TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway | R-HSA-5676594 | 8.739818e-01 | 0.058 | 0 | 0 |
| Processing of SMDT1 | R-HSA-8949664 | 8.739818e-01 | 0.058 | 0 | 0 |
| NFE2L2 regulating tumorigenic genes | R-HSA-9818030 | 8.739818e-01 | 0.058 | 0 | 0 |
| Replication of the SARS-CoV-1 genome | R-HSA-9682706 | 8.739818e-01 | 0.058 | 0 | 0 |
| BMAL1:CLOCK,NPAS2 activates circadian expression | R-HSA-1368108 | 8.750729e-01 | 0.058 | 0 | 0 |
| Signaling by NOTCH2 | R-HSA-1980145 | 8.750729e-01 | 0.058 | 0 | 0 |
| Antigen Presentation: Folding, assembly and peptide loading of class I MHC | R-HSA-983170 | 8.750729e-01 | 0.058 | 0 | 0 |
| NOD1/2 Signaling Pathway | R-HSA-168638 | 8.750729e-01 | 0.058 | 0 | 0 |
| Non-integrin membrane-ECM interactions | R-HSA-3000171 | 8.771399e-01 | 0.057 | 0 | 0 |
| TP53 Regulates Transcription of Cell Death Genes | R-HSA-5633008 | 8.771399e-01 | 0.057 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 8.796933e-01 | 0.056 | 0 | 0 |
| TRAF6 mediated NF-kB activation | R-HSA-933542 | 8.796933e-01 | 0.056 | 0 | 0 |
| Signaling by FLT3 ITD and TKD mutants | R-HSA-9703648 | 8.796933e-01 | 0.056 | 0 | 0 |
| Norepinephrine Neurotransmitter Release Cycle | R-HSA-181430 | 8.796933e-01 | 0.056 | 0 | 0 |
| Plasma lipoprotein assembly | R-HSA-8963898 | 8.796933e-01 | 0.056 | 0 | 0 |
| Assembly of active LPL and LIPC lipase complexes | R-HSA-8963889 | 8.796933e-01 | 0.056 | 0 | 0 |
| Downstream signaling of activated FGFR2 | R-HSA-5654696 | 8.850013e-01 | 0.053 | 0 | 0 |
| Downstream signaling of activated FGFR1 | R-HSA-5654687 | 8.850013e-01 | 0.053 | 0 | 0 |
| Ribosomal scanning and start codon recognition | R-HSA-72702 | 8.884179e-01 | 0.051 | 0 | 0 |
| Synthesis of IPs in the nucleus | R-HSA-1855191 | 8.884453e-01 | 0.051 | 0 | 0 |
| Beta oxidation of lauroyl-CoA to decanoyl-CoA-CoA | R-HSA-77310 | 8.884453e-01 | 0.051 | 0 | 0 |
| Beta oxidation of hexanoyl-CoA to butanoyl-CoA | R-HSA-77350 | 8.884453e-01 | 0.051 | 0 | 0 |
| Beta oxidation of octanoyl-CoA to hexanoyl-CoA | R-HSA-77348 | 8.884453e-01 | 0.051 | 0 | 0 |
| Formation of the active cofactor, UDP-glucuronate | R-HSA-173599 | 8.884453e-01 | 0.051 | 0 | 0 |
| MAP3K8 (TPL2)-dependent MAPK1/3 activation | R-HSA-5684264 | 8.884453e-01 | 0.051 | 0 | 0 |
| HDL assembly | R-HSA-8963896 | 8.884453e-01 | 0.051 | 0 | 0 |
| Acyl chain remodeling of CL | R-HSA-1482798 | 8.884453e-01 | 0.051 | 0 | 0 |
| P2Y receptors | R-HSA-417957 | 8.884453e-01 | 0.051 | 0 | 0 |
| Zinc transporters | R-HSA-435354 | 8.884453e-01 | 0.051 | 0 | 0 |
| SARS-CoV-1 Genome Replication and Transcription | R-HSA-9679514 | 8.884453e-01 | 0.051 | 0 | 0 |
| PI-3K cascade:FGFR2 | R-HSA-5654695 | 8.907184e-01 | 0.050 | 0 | 0 |
| FRS-mediated FGFR1 signaling | R-HSA-5654693 | 8.907184e-01 | 0.050 | 0 | 0 |
| Formation of the nephric duct | R-HSA-9830364 | 8.907184e-01 | 0.050 | 0 | 0 |
| MicroRNA (miRNA) biogenesis | R-HSA-203927 | 8.907184e-01 | 0.050 | 0 | 0 |
| Laminin interactions | R-HSA-3000157 | 8.907184e-01 | 0.050 | 0 | 0 |
| Cargo recognition for clathrin-mediated endocytosis | R-HSA-8856825 | 8.916613e-01 | 0.050 | 0 | 0 |
| Calmodulin induced events | R-HSA-111933 | 8.942189e-01 | 0.049 | 0 | 0 |
| CaM pathway | R-HSA-111997 | 8.942189e-01 | 0.049 | 0 | 0 |
| Triglyceride catabolism | R-HSA-163560 | 8.942189e-01 | 0.049 | 0 | 0 |
| Collagen biosynthesis and modifying enzymes | R-HSA-1650814 | 8.994932e-01 | 0.046 | 0 | 0 |
| MET activates PTK2 signaling | R-HSA-8874081 | 9.007985e-01 | 0.045 | 0 | 0 |
| Glutamate Neurotransmitter Release Cycle | R-HSA-210500 | 9.007985e-01 | 0.045 | 0 | 0 |
| Reproduction | R-HSA-1474165 | 9.009626e-01 | 0.045 | 0 | 0 |
| Adenylate cyclase inhibitory pathway | R-HSA-170670 | 9.012495e-01 | 0.045 | 0 | 0 |
| Beta-catenin phosphorylation cascade | R-HSA-196299 | 9.012495e-01 | 0.045 | 0 | 0 |
| RNA Polymerase III Chain Elongation | R-HSA-73780 | 9.012495e-01 | 0.045 | 0 | 0 |
| Sema3A PAK dependent Axon repulsion | R-HSA-399954 | 9.012495e-01 | 0.045 | 0 | 0 |
| SHC1 events in EGFR signaling | R-HSA-180336 | 9.012495e-01 | 0.045 | 0 | 0 |
| ERBB2 Regulates Cell Motility | R-HSA-6785631 | 9.012495e-01 | 0.045 | 0 | 0 |
| Transport and metabolism of PAPS | R-HSA-174362 | 9.012495e-01 | 0.045 | 0 | 0 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | R-HSA-450513 | 9.012495e-01 | 0.045 | 0 | 0 |
| Lysosphingolipid and LPA receptors | R-HSA-419408 | 9.012495e-01 | 0.045 | 0 | 0 |
| Protein methylation | R-HSA-8876725 | 9.012495e-01 | 0.045 | 0 | 0 |
| DNA Damage Reversal | R-HSA-73942 | 9.012495e-01 | 0.045 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 9.014478e-01 | 0.045 | 0 | 0 |
| Synthesis of PC | R-HSA-1483191 | 9.014478e-01 | 0.045 | 0 | 0 |
| Unfolded Protein Response (UPR) | R-HSA-381119 | 9.026074e-01 | 0.045 | 0 | 0 |
| TRAF6 mediated IRF7 activation | R-HSA-933541 | 9.027671e-01 | 0.044 | 0 | 0 |
| Metabolism of folate and pterines | R-HSA-196757 | 9.027671e-01 | 0.044 | 0 | 0 |
| Telomere Maintenance | R-HSA-157579 | 9.077419e-01 | 0.042 | 0 | 0 |
| RNA Polymerase I Promoter Opening | R-HSA-73728 | 9.100052e-01 | 0.041 | 0 | 0 |
| Packaging Of Telomere Ends | R-HSA-171306 | 9.100052e-01 | 0.041 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 9.100052e-01 | 0.041 | 0 | 0 |
| TNFR1-induced NF-kappa-B signaling pathway | R-HSA-5357956 | 9.100052e-01 | 0.041 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 9.106861e-01 | 0.041 | 0 | 0 |
| SLC-mediated transport of inorganic anions | R-HSA-9958790 | 9.106861e-01 | 0.041 | 0 | 0 |
| Class I peroxisomal membrane protein import | R-HSA-9603798 | 9.125847e-01 | 0.040 | 0 | 0 |
| WNT5A-dependent internalization of FZD4 | R-HSA-5099900 | 9.125847e-01 | 0.040 | 0 | 0 |
| Stimuli-sensing channels | R-HSA-2672351 | 9.174020e-01 | 0.037 | 0 | 0 |
| Cargo trafficking to the periciliary membrane | R-HSA-5620920 | 9.176410e-01 | 0.037 | 0 | 0 |
| FRS-mediated FGFR2 signaling | R-HSA-5654700 | 9.184061e-01 | 0.037 | 0 | 0 |
| ATF4 activates genes in response to endoplasmic reticulum stress | R-HSA-380994 | 9.184061e-01 | 0.037 | 0 | 0 |
| Signaling by FGFR2 in disease | R-HSA-5655253 | 9.218360e-01 | 0.035 | 0 | 0 |
| POU5F1 (OCT4), SOX2, NANOG activate genes related to proliferation | R-HSA-2892247 | 9.226194e-01 | 0.035 | 0 | 0 |
| G beta:gamma signalling through CDC42 | R-HSA-8964616 | 9.226194e-01 | 0.035 | 0 | 0 |
| GRB2 events in ERBB2 signaling | R-HSA-1963640 | 9.226194e-01 | 0.035 | 0 | 0 |
| TRAF6 mediated IRF7 activation in TLR7/8 or 9 signaling | R-HSA-975110 | 9.226194e-01 | 0.035 | 0 | 0 |
| SHC1 events in ERBB4 signaling | R-HSA-1250347 | 9.226194e-01 | 0.035 | 0 | 0 |
| mitochondrial fatty acid beta-oxidation of unsaturated fatty acids | R-HSA-77288 | 9.226194e-01 | 0.035 | 0 | 0 |
| STAT5 activation downstream of FLT3 ITD mutants | R-HSA-9702518 | 9.226194e-01 | 0.035 | 0 | 0 |
| Regulation of innate immune responses to cytosolic DNA | R-HSA-3134975 | 9.226194e-01 | 0.035 | 0 | 0 |
| Beta oxidation of decanoyl-CoA to octanoyl-CoA-CoA | R-HSA-77346 | 9.226194e-01 | 0.035 | 0 | 0 |
| Scavenging by Class B Receptors | R-HSA-3000471 | 9.226194e-01 | 0.035 | 0 | 0 |
| Synthesis of PG | R-HSA-1483148 | 9.226194e-01 | 0.035 | 0 | 0 |
| Acetylcholine regulates insulin secretion | R-HSA-399997 | 9.226194e-01 | 0.035 | 0 | 0 |
| Coenzyme A biosynthesis | R-HSA-196783 | 9.226194e-01 | 0.035 | 0 | 0 |
| tRNA modification in the mitochondrion | R-HSA-6787450 | 9.226194e-01 | 0.035 | 0 | 0 |
| TFAP2 (AP-2) family regulates transcription of growth factors and their receptors | R-HSA-8866910 | 9.226194e-01 | 0.035 | 0 | 0 |
| trans-Golgi Network Vesicle Budding | R-HSA-199992 | 9.230201e-01 | 0.035 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 9.248834e-01 | 0.034 | 0 | 0 |
| Toll-like Receptor Cascades | R-HSA-168898 | 9.259822e-01 | 0.033 | 0 | 0 |
| Regulation of gene expression in beta cells | R-HSA-210745 | 9.260648e-01 | 0.033 | 0 | 0 |
| Signaling by CSF3 (G-CSF) | R-HSA-9674555 | 9.260648e-01 | 0.033 | 0 | 0 |
| Platelet calcium homeostasis | R-HSA-418360 | 9.260648e-01 | 0.033 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 9.261118e-01 | 0.033 | 0 | 0 |
| NCAM signaling for neurite out-growth | R-HSA-375165 | 9.271429e-01 | 0.033 | 0 | 0 |
| Meiotic recombination | R-HSA-912446 | 9.277394e-01 | 0.033 | 0 | 0 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | R-HSA-1445148 | 9.280885e-01 | 0.032 | 0 | 0 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | R-HSA-166058 | 9.298739e-01 | 0.032 | 0 | 0 |
| Toll Like Receptor TLR6:TLR2 Cascade | R-HSA-168188 | 9.298739e-01 | 0.032 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 9.304982e-01 | 0.031 | 0 | 0 |
| Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 | R-HSA-5625886 | 9.310489e-01 | 0.031 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 9.313632e-01 | 0.031 | 0 | 0 |
| Sulfide oxidation to sulfate | R-HSA-1614517 | 9.315026e-01 | 0.031 | 0 | 0 |
| PI3K events in ERBB2 signaling | R-HSA-1963642 | 9.315026e-01 | 0.031 | 0 | 0 |
| Glycogen storage diseases | R-HSA-3229121 | 9.315026e-01 | 0.031 | 0 | 0 |
| Metabolism of ingested H2SeO4 and H2SeO3 into H2Se | R-HSA-2408550 | 9.315026e-01 | 0.031 | 0 | 0 |
| Modulation of host responses by IFN-stimulated genes | R-HSA-9909505 | 9.315026e-01 | 0.031 | 0 | 0 |
| Replication of the SARS-CoV-2 genome | R-HSA-9694686 | 9.315026e-01 | 0.031 | 0 | 0 |
| rRNA modification in the nucleus and cytosol | R-HSA-6790901 | 9.322834e-01 | 0.030 | 0 | 0 |
| G1/S DNA Damage Checkpoints | R-HSA-69615 | 9.322834e-01 | 0.030 | 0 | 0 |
| Signaling by ERBB4 | R-HSA-1236394 | 9.328603e-01 | 0.030 | 0 | 0 |
| DAP12 signaling | R-HSA-2424491 | 9.330411e-01 | 0.030 | 0 | 0 |
| SHC1 events in ERBB2 signaling | R-HSA-1250196 | 9.330411e-01 | 0.030 | 0 | 0 |
| SARS-CoV-1 activates/modulates innate immune responses | R-HSA-9692916 | 9.332375e-01 | 0.030 | 0 | 0 |
| Translation of Structural Proteins | R-HSA-9683701 | 9.368246e-01 | 0.028 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 9.387342e-01 | 0.027 | 0 | 0 |
| Trafficking of GluR2-containing AMPA receptors | R-HSA-416993 | 9.393666e-01 | 0.027 | 0 | 0 |
| Chaperone Mediated Autophagy | R-HSA-9613829 | 9.393666e-01 | 0.027 | 0 | 0 |
| Cytosolic iron-sulfur cluster assembly | R-HSA-2564830 | 9.393666e-01 | 0.027 | 0 | 0 |
| Organic anion transport by SLC5/17/25 transporters | R-HSA-428643 | 9.393666e-01 | 0.027 | 0 | 0 |
| Apoptotic factor-mediated response | R-HSA-111471 | 9.393666e-01 | 0.027 | 0 | 0 |
| Nucleotide-like (purinergic) receptors | R-HSA-418038 | 9.393666e-01 | 0.027 | 0 | 0 |
| Vitamin D (calciferol) metabolism | R-HSA-196791 | 9.393666e-01 | 0.027 | 0 | 0 |
| Evasion by RSV of host interferon responses | R-HSA-9833109 | 9.393906e-01 | 0.027 | 0 | 0 |
| Toll Like Receptor TLR1:TLR2 Cascade | R-HSA-168179 | 9.406071e-01 | 0.027 | 0 | 0 |
| Toll Like Receptor 2 (TLR2) Cascade | R-HSA-181438 | 9.406071e-01 | 0.027 | 0 | 0 |
| Glucagon-like Peptide-1 (GLP1) regulates insulin secretion | R-HSA-381676 | 9.421502e-01 | 0.026 | 0 | 0 |
| Ca-dependent events | R-HSA-111996 | 9.421502e-01 | 0.026 | 0 | 0 |
| Base-Excision Repair, AP Site Formation | R-HSA-73929 | 9.431108e-01 | 0.025 | 0 | 0 |
| Developmental Lineage of Multipotent Pancreatic Progenitor Cells | R-HSA-9937080 | 9.451652e-01 | 0.024 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected purine | R-HSA-110330 | 9.451652e-01 | 0.024 | 0 | 0 |
| NR1H2 and NR1H3-mediated signaling | R-HSA-9024446 | 9.455343e-01 | 0.024 | 0 | 0 |
| Pre-NOTCH Processing in Golgi | R-HSA-1912420 | 9.463281e-01 | 0.024 | 0 | 0 |
| Crosslinking of collagen fibrils | R-HSA-2243919 | 9.463281e-01 | 0.024 | 0 | 0 |
| Signaling by FGFR2 IIIa TM | R-HSA-8851708 | 9.463281e-01 | 0.024 | 0 | 0 |
| mRNA decay by 3' to 5' exoribonuclease | R-HSA-429958 | 9.463281e-01 | 0.024 | 0 | 0 |
| Specification of the neural plate border | R-HSA-9834899 | 9.463281e-01 | 0.024 | 0 | 0 |
| Gastrin-CREB signalling pathway via PKC and MAPK | R-HSA-881907 | 9.463281e-01 | 0.024 | 0 | 0 |
| Diseases of hemostasis | R-HSA-9671793 | 9.463281e-01 | 0.024 | 0 | 0 |
| Methionine salvage pathway | R-HSA-1237112 | 9.463281e-01 | 0.024 | 0 | 0 |
| HDL remodeling | R-HSA-8964058 | 9.463281e-01 | 0.024 | 0 | 0 |
| Strand-asynchronous mitochondrial DNA replication | R-HSA-9913635 | 9.463281e-01 | 0.024 | 0 | 0 |
| SARS-CoV-2 Genome Replication and Transcription | R-HSA-9694682 | 9.463281e-01 | 0.024 | 0 | 0 |
| Response of Mtb to phagocytosis | R-HSA-9637690 | 9.470567e-01 | 0.024 | 0 | 0 |
| TP53 Regulates Metabolic Genes | R-HSA-5628897 | 9.477480e-01 | 0.023 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 9.489504e-01 | 0.023 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 9.489699e-01 | 0.023 | 0 | 0 |
| Kidney development | R-HSA-9830369 | 9.497476e-01 | 0.022 | 0 | 0 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | R-HSA-9668328 | 9.504132e-01 | 0.022 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 9.511670e-01 | 0.022 | 0 | 0 |
| SCF(Skp2)-mediated degradation of p27/p21 | R-HSA-187577 | 9.515735e-01 | 0.022 | 0 | 0 |
| Amine ligand-binding receptors | R-HSA-375280 | 9.515735e-01 | 0.022 | 0 | 0 |
| Gap junction trafficking | R-HSA-190828 | 9.515735e-01 | 0.022 | 0 | 0 |
| Formation of definitive endoderm | R-HSA-9823730 | 9.524907e-01 | 0.021 | 0 | 0 |
| Glycogen synthesis | R-HSA-3322077 | 9.524907e-01 | 0.021 | 0 | 0 |
| Co-inhibition by CTLA4 | R-HSA-389513 | 9.524907e-01 | 0.021 | 0 | 0 |
| Acyl chain remodelling of PI | R-HSA-1482922 | 9.524907e-01 | 0.021 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 9.524907e-01 | 0.021 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 9.536013e-01 | 0.021 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 9.536013e-01 | 0.021 | 0 | 0 |
| Signaling by FGFR | R-HSA-190236 | 9.537335e-01 | 0.021 | 0 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 9.546928e-01 | 0.020 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 9.548960e-01 | 0.020 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 9.548960e-01 | 0.020 | 0 | 0 |
| Striated Muscle Contraction | R-HSA-390522 | 9.551795e-01 | 0.020 | 0 | 0 |
| Glucagon signaling in metabolic regulation | R-HSA-163359 | 9.551795e-01 | 0.020 | 0 | 0 |
| Effects of PIP2 hydrolysis | R-HSA-114508 | 9.551795e-01 | 0.020 | 0 | 0 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | R-HSA-9768727 | 9.551795e-01 | 0.020 | 0 | 0 |
| Vasopressin regulates renal water homeostasis via Aquaporins | R-HSA-432040 | 9.557284e-01 | 0.020 | 0 | 0 |
| DAG and IP3 signaling | R-HSA-1489509 | 9.557284e-01 | 0.020 | 0 | 0 |
| Glucose metabolism | R-HSA-70326 | 9.563044e-01 | 0.019 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 9.566514e-01 | 0.019 | 0 | 0 |
| SHC-mediated cascade:FGFR3 | R-HSA-5654704 | 9.579460e-01 | 0.019 | 0 | 0 |
| Prevention of phagosomal-lysosomal fusion | R-HSA-9636383 | 9.579460e-01 | 0.019 | 0 | 0 |
| Early SARS-CoV-2 Infection Events | R-HSA-9772572 | 9.589662e-01 | 0.018 | 0 | 0 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | R-HSA-6814122 | 9.595053e-01 | 0.018 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 9.617600e-01 | 0.017 | 0 | 0 |
| Regulation of beta-cell development | R-HSA-186712 | 9.622338e-01 | 0.017 | 0 | 0 |
| HCMV Early Events | R-HSA-9609690 | 9.627092e-01 | 0.017 | 0 | 0 |
| Inactivation of CSF3 (G-CSF) signaling | R-HSA-9705462 | 9.627752e-01 | 0.016 | 0 | 0 |
| SHC-mediated cascade:FGFR4 | R-HSA-5654719 | 9.627752e-01 | 0.016 | 0 | 0 |
| Molybdenum cofactor biosynthesis | R-HSA-947581 | 9.627752e-01 | 0.016 | 0 | 0 |
| Glutathione synthesis and recycling | R-HSA-174403 | 9.627752e-01 | 0.016 | 0 | 0 |
| HCMV Late Events | R-HSA-9610379 | 9.629119e-01 | 0.016 | 0 | 0 |
| TAK1-dependent IKK and NF-kappa-B activation | R-HSA-445989 | 9.630558e-01 | 0.016 | 0 | 0 |
| SCF-beta-TrCP mediated degradation of Emi1 | R-HSA-174113 | 9.634290e-01 | 0.016 | 0 | 0 |
| PERK regulates gene expression | R-HSA-381042 | 9.634290e-01 | 0.016 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 9.642667e-01 | 0.016 | 0 | 0 |
| Late SARS-CoV-2 Infection Events | R-HSA-9772573 | 9.642667e-01 | 0.016 | 0 | 0 |
| Glutathione conjugation | R-HSA-156590 | 9.652585e-01 | 0.015 | 0 | 0 |
| GPER1 signaling | R-HSA-9634597 | 9.662760e-01 | 0.015 | 0 | 0 |
| Lysosome Vesicle Biogenesis | R-HSA-432720 | 9.669859e-01 | 0.015 | 0 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 9.669859e-01 | 0.015 | 0 | 0 |
| RNA Polymerase III Transcription Initiation From Type 3 Promoter | R-HSA-76071 | 9.670501e-01 | 0.015 | 0 | 0 |
| Cholesterol biosynthesis via lathosterol | R-HSA-6807062 | 9.670501e-01 | 0.015 | 0 | 0 |
| Cellular hexose transport | R-HSA-189200 | 9.670501e-01 | 0.015 | 0 | 0 |
| LDL clearance | R-HSA-8964038 | 9.670501e-01 | 0.015 | 0 | 0 |
| Nucleotide salvage | R-HSA-8956321 | 9.680565e-01 | 0.014 | 0 | 0 |
| Ca2+ pathway | R-HSA-4086398 | 9.683707e-01 | 0.014 | 0 | 0 |
| SIRT1 negatively regulates rRNA expression | R-HSA-427359 | 9.702084e-01 | 0.013 | 0 | 0 |
| Cleavage of the damaged purine | R-HSA-110331 | 9.702084e-01 | 0.013 | 0 | 0 |
| SLC-mediated transport of organic cations | R-HSA-549127 | 9.702084e-01 | 0.013 | 0 | 0 |
| Signaling by NOTCH4 | R-HSA-9013694 | 9.707688e-01 | 0.013 | 0 | 0 |
| Prefoldin mediated transfer of substrate to CCT/TriC | R-HSA-389957 | 9.708343e-01 | 0.013 | 0 | 0 |
| Response of EIF2AK1 (HRI) to heme deficiency | R-HSA-9648895 | 9.708343e-01 | 0.013 | 0 | 0 |
| Interleukin-20 family signaling | R-HSA-8854691 | 9.708343e-01 | 0.013 | 0 | 0 |
| Free fatty acids regulate insulin secretion | R-HSA-400451 | 9.708343e-01 | 0.013 | 0 | 0 |
| Organic anion transport by SLCO transporters | R-HSA-879518 | 9.708343e-01 | 0.013 | 0 | 0 |
| Formation of the ureteric bud | R-HSA-9830674 | 9.708343e-01 | 0.013 | 0 | 0 |
| Regulation of RAS by GAPs | R-HSA-5658442 | 9.719380e-01 | 0.012 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 9.719380e-01 | 0.012 | 0 | 0 |
| Transcriptional regulation of pluripotent stem cells | R-HSA-452723 | 9.731265e-01 | 0.012 | 0 | 0 |
| Depurination | R-HSA-73927 | 9.731265e-01 | 0.012 | 0 | 0 |
| Metabolism of nitric oxide: NOS3 activation and regulation | R-HSA-202131 | 9.731265e-01 | 0.012 | 0 | 0 |
| Formation of tubulin folding intermediates by CCT/TriC | R-HSA-389960 | 9.741841e-01 | 0.011 | 0 | 0 |
| SHC-mediated cascade:FGFR1 | R-HSA-5654688 | 9.741841e-01 | 0.011 | 0 | 0 |
| Replacement of protamines by nucleosomes in the male pronucleus | R-HSA-9821993 | 9.741841e-01 | 0.011 | 0 | 0 |
| ADP signalling through P2Y purinoceptor 1 | R-HSA-418592 | 9.741841e-01 | 0.011 | 0 | 0 |
| CD209 (DC-SIGN) signaling | R-HSA-5621575 | 9.741841e-01 | 0.011 | 0 | 0 |
| TNFs bind their physiological receptors | R-HSA-5669034 | 9.741841e-01 | 0.011 | 0 | 0 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | R-HSA-1234176 | 9.744190e-01 | 0.011 | 0 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 9.750672e-01 | 0.011 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 9.756469e-01 | 0.011 | 0 | 0 |
| Stabilization of p53 | R-HSA-69541 | 9.757674e-01 | 0.011 | 0 | 0 |
| Plasma lipoprotein clearance | R-HSA-8964043 | 9.757674e-01 | 0.011 | 0 | 0 |
| AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | R-HSA-9931269 | 9.766907e-01 | 0.010 | 0 | 0 |
| Translation of Structural Proteins | R-HSA-9694635 | 9.769885e-01 | 0.010 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 9.770943e-01 | 0.010 | 0 | 0 |
| Tight junction interactions | R-HSA-420029 | 9.771493e-01 | 0.010 | 0 | 0 |
| Hyaluronan degradation | R-HSA-2160916 | 9.771493e-01 | 0.010 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 9.771493e-01 | 0.010 | 0 | 0 |
| Fertilization | R-HSA-1187000 | 9.771493e-01 | 0.010 | 0 | 0 |
| VEGFR2 mediated cell proliferation | R-HSA-5218921 | 9.771493e-01 | 0.010 | 0 | 0 |
| PIWI-interacting RNA (piRNA) biogenesis | R-HSA-5601884 | 9.771493e-01 | 0.010 | 0 | 0 |
| Glycogen breakdown (glycogenolysis) | R-HSA-70221 | 9.771493e-01 | 0.010 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 9.772747e-01 | 0.010 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 9.774263e-01 | 0.010 | 0 | 0 |
| Regulation of RUNX3 expression and activity | R-HSA-8941858 | 9.781565e-01 | 0.010 | 0 | 0 |
| Glycogen metabolism | R-HSA-8982491 | 9.781565e-01 | 0.010 | 0 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 9.781565e-01 | 0.010 | 0 | 0 |
| Amino acids regulate mTORC1 | R-HSA-9639288 | 9.787696e-01 | 0.009 | 0 | 0 |
| SLC-mediated transport of organic anions | R-HSA-9955298 | 9.787708e-01 | 0.009 | 0 | 0 |
| Adrenaline,noradrenaline inhibits insulin secretion | R-HSA-400042 | 9.797741e-01 | 0.009 | 0 | 0 |
| Metalloprotease DUBs | R-HSA-5689901 | 9.797741e-01 | 0.009 | 0 | 0 |
| TRP channels | R-HSA-3295583 | 9.797741e-01 | 0.009 | 0 | 0 |
| Urea cycle | R-HSA-70635 | 9.797741e-01 | 0.009 | 0 | 0 |
| Sphingolipid catabolism | R-HSA-9845614 | 9.797741e-01 | 0.009 | 0 | 0 |
| Synthesis of IP2, IP, and Ins in the cytosol | R-HSA-1855183 | 9.797741e-01 | 0.009 | 0 | 0 |
| Suppression of phagosomal maturation | R-HSA-9637687 | 9.797741e-01 | 0.009 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 9.800874e-01 | 0.009 | 1 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 9.803166e-01 | 0.009 | 0 | 0 |
| Purine ribonucleoside monophosphate biosynthesis | R-HSA-73817 | 9.803166e-01 | 0.009 | 0 | 0 |
| Maturation of spike protein | R-HSA-9694548 | 9.803166e-01 | 0.009 | 0 | 0 |
| SARS-CoV-2 modulates host translation machinery | R-HSA-9754678 | 9.806710e-01 | 0.008 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 9.817107e-01 | 0.008 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 9.820662e-01 | 0.008 | 0 | 0 |
| SHC-mediated cascade:FGFR2 | R-HSA-5654699 | 9.820975e-01 | 0.008 | 0 | 0 |
| Cristae formation | R-HSA-8949613 | 9.820975e-01 | 0.008 | 0 | 0 |
| Signaling by BMP | R-HSA-201451 | 9.820975e-01 | 0.008 | 0 | 0 |
| Phosphorylation of CD3 and TCR zeta chains | R-HSA-202427 | 9.820975e-01 | 0.008 | 0 | 0 |
| ER Quality Control Compartment (ERQC) | R-HSA-901032 | 9.820975e-01 | 0.008 | 0 | 0 |
| Synthesis of bile acids and bile salts via 27-hydroxycholesterol | R-HSA-193807 | 9.820975e-01 | 0.008 | 0 | 0 |
| Insulin processing | R-HSA-264876 | 9.820975e-01 | 0.008 | 0 | 0 |
| Degradation of CRY and PER proteins | R-HSA-9932298 | 9.822688e-01 | 0.008 | 0 | 0 |
| SLC-mediated transport of neurotransmitters | R-HSA-442660 | 9.822688e-01 | 0.008 | 0 | 0 |
| HCMV Infection | R-HSA-9609646 | 9.823528e-01 | 0.008 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 9.824767e-01 | 0.008 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 9.825728e-01 | 0.008 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 9.828183e-01 | 0.008 | 0 | 0 |
| tRNA processing | R-HSA-72306 | 9.831880e-01 | 0.007 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 9.833185e-01 | 0.007 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 9.833185e-01 | 0.007 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 9.834037e-01 | 0.007 | 0 | 0 |
| Neddylation | R-HSA-8951664 | 9.834779e-01 | 0.007 | 0 | 0 |
| Detoxification of Reactive Oxygen Species | R-HSA-3299685 | 9.839970e-01 | 0.007 | 0 | 0 |
| Telomere Extension By Telomerase | R-HSA-171319 | 9.841542e-01 | 0.007 | 0 | 0 |
| Insulin receptor recycling | R-HSA-77387 | 9.841542e-01 | 0.007 | 0 | 0 |
| Pyroptosis | R-HSA-5620971 | 9.841542e-01 | 0.007 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 9.850599e-01 | 0.007 | 0 | 0 |
| Fatty acyl-CoA biosynthesis | R-HSA-75105 | 9.852949e-01 | 0.006 | 0 | 0 |
| Synthesis of PA | R-HSA-1483166 | 9.854471e-01 | 0.006 | 0 | 0 |
| Hedgehog 'on' state | R-HSA-5632684 | 9.865370e-01 | 0.006 | 0 | 0 |
| Transcriptional and post-translational regulation of MITF-M expression and activity | R-HSA-9856649 | 9.865370e-01 | 0.006 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 9.870625e-01 | 0.006 | 0 | 0 |
| RSV-host interactions | R-HSA-9833110 | 9.870676e-01 | 0.006 | 0 | 0 |
| Thrombin signalling through proteinase activated receptors (PARs) | R-HSA-456926 | 9.875861e-01 | 0.005 | 0 | 0 |
| Neurotransmitter clearance | R-HSA-112311 | 9.875861e-01 | 0.005 | 0 | 0 |
| Mucopolysaccharidoses | R-HSA-2206281 | 9.875861e-01 | 0.005 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 9.878744e-01 | 0.005 | 0 | 0 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | R-HSA-168928 | 9.878744e-01 | 0.005 | 0 | 0 |
| Peroxisomal protein import | R-HSA-9033241 | 9.879781e-01 | 0.005 | 0 | 0 |
| Amino acid transport across the plasma membrane | R-HSA-352230 | 9.879781e-01 | 0.005 | 0 | 0 |
| Triglyceride metabolism | R-HSA-8979227 | 9.879781e-01 | 0.005 | 0 | 0 |
| Interferon alpha/beta signaling | R-HSA-909733 | 9.883539e-01 | 0.005 | 0 | 0 |
| ADORA2B mediated anti-inflammatory cytokines production | R-HSA-9660821 | 9.883595e-01 | 0.005 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 9.887999e-01 | 0.005 | 0 | 0 |
| Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | R-HSA-9954709 | 9.887999e-01 | 0.005 | 0 | 0 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | R-HSA-389958 | 9.890124e-01 | 0.005 | 0 | 0 |
| Respiratory syncytial virus (RSV) attachment and entry | R-HSA-9820960 | 9.890124e-01 | 0.005 | 0 | 0 |
| Molecules associated with elastic fibres | R-HSA-2129379 | 9.890124e-01 | 0.005 | 0 | 0 |
| Formation of the ternary complex, and subsequently, the 43S complex | R-HSA-72695 | 9.895294e-01 | 0.005 | 0 | 0 |
| Regulation of pyruvate metabolism | R-HSA-9861718 | 9.895294e-01 | 0.005 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 9.896996e-01 | 0.004 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 9.900030e-01 | 0.004 | 0 | 0 |
| Aquaporin-mediated transport | R-HSA-445717 | 9.900828e-01 | 0.004 | 0 | 0 |
| PLC beta mediated events | R-HSA-112043 | 9.900828e-01 | 0.004 | 0 | 0 |
| HS-GAG degradation | R-HSA-2024096 | 9.902750e-01 | 0.004 | 0 | 0 |
| DAG1 glycosylations | R-HSA-8931838 | 9.902750e-01 | 0.004 | 0 | 0 |
| G-protein beta:gamma signalling | R-HSA-397795 | 9.913925e-01 | 0.004 | 0 | 0 |
| Recycling of bile acids and salts | R-HSA-159418 | 9.913925e-01 | 0.004 | 0 | 0 |
| Plasma lipoprotein remodeling | R-HSA-8963899 | 9.915350e-01 | 0.004 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 9.918208e-01 | 0.004 | 0 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 9.919495e-01 | 0.004 | 0 | 0 |
| Leishmania phagocytosis | R-HSA-9664417 | 9.919495e-01 | 0.004 | 0 | 0 |
| Parasite infection | R-HSA-9664407 | 9.919495e-01 | 0.004 | 0 | 0 |
| Acyl chain remodelling of PC | R-HSA-1482788 | 9.923817e-01 | 0.003 | 0 | 0 |
| Heme degradation | R-HSA-189483 | 9.923817e-01 | 0.003 | 0 | 0 |
| Glutamate and glutamine metabolism | R-HSA-8964539 | 9.923817e-01 | 0.003 | 0 | 0 |
| Vitamin B5 (pantothenate) metabolism | R-HSA-199220 | 9.923817e-01 | 0.003 | 0 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 9.923916e-01 | 0.003 | 0 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 9.924908e-01 | 0.003 | 0 | 0 |
| Nuclear events mediated by NFE2L2 | R-HSA-9759194 | 9.925187e-01 | 0.003 | 0 | 0 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | R-HSA-168643 | 9.925879e-01 | 0.003 | 0 | 0 |
| Cholesterol biosynthesis | R-HSA-191273 | 9.928152e-01 | 0.003 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 9.932277e-01 | 0.003 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 9.932573e-01 | 0.003 | 0 | 0 |
| Hyaluronan metabolism | R-HSA-2142845 | 9.932573e-01 | 0.003 | 0 | 0 |
| Calnexin/calreticulin cycle | R-HSA-901042 | 9.932573e-01 | 0.003 | 0 | 0 |
| Signal amplification | R-HSA-392518 | 9.932573e-01 | 0.003 | 0 | 0 |
| Cellular response to hypoxia | R-HSA-1234174 | 9.932777e-01 | 0.003 | 0 | 0 |
| Cytosolic sulfonation of small molecules | R-HSA-156584 | 9.938580e-01 | 0.003 | 0 | 0 |
| tRNA modification in the nucleus and cytosol | R-HSA-6782315 | 9.939051e-01 | 0.003 | 0 | 0 |
| Acyl chain remodelling of PE | R-HSA-1482839 | 9.940322e-01 | 0.003 | 0 | 0 |
| Defects in vitamin and cofactor metabolism | R-HSA-3296482 | 9.940322e-01 | 0.003 | 0 | 0 |
| Plasma lipoprotein assembly, remodeling, and clearance | R-HSA-174824 | 9.944546e-01 | 0.002 | 0 | 0 |
| G-protein mediated events | R-HSA-112040 | 9.944756e-01 | 0.002 | 0 | 0 |
| SLC-mediated transport of amino acids | R-HSA-9958863 | 9.944756e-01 | 0.002 | 0 | 0 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | R-HSA-450408 | 9.947182e-01 | 0.002 | 0 | 0 |
| FGFR2 mutant receptor activation | R-HSA-1839126 | 9.947182e-01 | 0.002 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 9.950464e-01 | 0.002 | 0 | 0 |
| Nucleotide biosynthesis | R-HSA-8956320 | 9.950464e-01 | 0.002 | 0 | 0 |
| Integration of energy metabolism | R-HSA-163685 | 9.953057e-01 | 0.002 | 0 | 0 |
| Degradation of DVL | R-HSA-4641258 | 9.953253e-01 | 0.002 | 0 | 0 |
| Beta-oxidation of very long chain fatty acids | R-HSA-390247 | 9.953253e-01 | 0.002 | 0 | 0 |
| NCAM1 interactions | R-HSA-419037 | 9.953253e-01 | 0.002 | 0 | 0 |
| Neurotransmitter receptors and postsynaptic signal transmission | R-HSA-112314 | 9.954425e-01 | 0.002 | 0 | 0 |
| Cytoprotection by HMOX1 | R-HSA-9707564 | 9.954579e-01 | 0.002 | 0 | 0 |
| Developmental Lineage of Pancreatic Ductal Cells | R-HSA-9925563 | 9.954653e-01 | 0.002 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 9.957819e-01 | 0.002 | 0 | 0 |
| Elastic fibre formation | R-HSA-1566948 | 9.958627e-01 | 0.002 | 0 | 0 |
| Purine salvage | R-HSA-74217 | 9.958627e-01 | 0.002 | 0 | 0 |
| Degradation of beta-catenin by the destruction complex | R-HSA-195253 | 9.958932e-01 | 0.002 | 0 | 0 |
| Downstream signaling events of B Cell Receptor (BCR) | R-HSA-1168372 | 9.958932e-01 | 0.002 | 0 | 0 |
| Cytosolic sensors of pathogen-associated DNA | R-HSA-1834949 | 9.958932e-01 | 0.002 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 9.959541e-01 | 0.002 | 0 | 0 |
| G alpha (z) signalling events | R-HSA-418597 | 9.960082e-01 | 0.002 | 0 | 0 |
| Gastrulation | R-HSA-9758941 | 9.960394e-01 | 0.002 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 9.960894e-01 | 0.002 | 0 | 0 |
| Ion homeostasis | R-HSA-5578775 | 9.964178e-01 | 0.002 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 9.964190e-01 | 0.002 | 0 | 0 |
| Potassium Channels | R-HSA-1296071 | 9.964190e-01 | 0.002 | 0 | 0 |
| Developmental Cell Lineages of the Integumentary System | R-HSA-9734779 | 9.964435e-01 | 0.002 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 9.965629e-01 | 0.001 | 0 | 0 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | R-HSA-450531 | 9.966345e-01 | 0.001 | 0 | 0 |
| Negative regulation of NOTCH4 signaling | R-HSA-9604323 | 9.967593e-01 | 0.001 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 9.967860e-01 | 0.001 | 0 | 0 |
| Regulation of insulin secretion | R-HSA-422356 | 9.970000e-01 | 0.001 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 9.971319e-01 | 0.001 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 9.971499e-01 | 0.001 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 9.973266e-01 | 0.001 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 9.974537e-01 | 0.001 | 0 | 0 |
| GLI3 is processed to GLI3R by the proteasome | R-HSA-5610785 | 9.974617e-01 | 0.001 | 0 | 0 |
| Degradation of GLI1 by the proteasome | R-HSA-5610780 | 9.974617e-01 | 0.001 | 0 | 0 |
| Scavenging by Class A Receptors | R-HSA-3000480 | 9.974617e-01 | 0.001 | 0 | 0 |
| Heme biosynthesis | R-HSA-189451 | 9.974617e-01 | 0.001 | 0 | 0 |
| SLC transporter disorders | R-HSA-5619102 | 9.974993e-01 | 0.001 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 9.977045e-01 | 0.001 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 9.977511e-01 | 0.001 | 0 | 0 |
| Activation of GABAB receptors | R-HSA-991365 | 9.977535e-01 | 0.001 | 0 | 0 |
| GABA B receptor activation | R-HSA-977444 | 9.977535e-01 | 0.001 | 0 | 0 |
| Cytosolic tRNA aminoacylation | R-HSA-379716 | 9.977535e-01 | 0.001 | 0 | 0 |
| Neurotransmitter release cycle | R-HSA-112310 | 9.978523e-01 | 0.001 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 9.979091e-01 | 0.001 | 0 | 0 |
| Glycerophospholipid biosynthesis | R-HSA-1483206 | 9.979183e-01 | 0.001 | 0 | 0 |
| Formation of paraxial mesoderm | R-HSA-9793380 | 9.979211e-01 | 0.001 | 0 | 0 |
| Synthesis of very long-chain fatty acyl-CoAs | R-HSA-75876 | 9.980119e-01 | 0.001 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 9.980822e-01 | 0.001 | 0 | 0 |
| Mitochondrial protein import | R-HSA-1268020 | 9.981365e-01 | 0.001 | 0 | 0 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | R-HSA-2142691 | 9.982405e-01 | 0.001 | 0 | 0 |
| Surfactant metabolism | R-HSA-5683826 | 9.982405e-01 | 0.001 | 0 | 0 |
| Opioid Signalling | R-HSA-111885 | 9.982478e-01 | 0.001 | 0 | 0 |
| Complex I biogenesis | R-HSA-6799198 | 9.983299e-01 | 0.001 | 0 | 0 |
| Developmental Lineage of Pancreatic Acinar Cells | R-HSA-9925561 | 9.983363e-01 | 0.001 | 0 | 0 |
| Protein folding | R-HSA-391251 | 9.983854e-01 | 0.001 | 0 | 0 |
| Defective CFTR causes cystic fibrosis | R-HSA-5678895 | 9.984429e-01 | 0.001 | 0 | 0 |
| mitochondrial fatty acid beta-oxidation of saturated fatty acids | R-HSA-77286 | 9.984429e-01 | 0.001 | 0 | 0 |
| Somitogenesis | R-HSA-9824272 | 9.984429e-01 | 0.001 | 0 | 0 |
| Asymmetric localization of PCP proteins | R-HSA-4608870 | 9.984429e-01 | 0.001 | 0 | 0 |
| Degradation of cysteine and homocysteine | R-HSA-1614558 | 9.984429e-01 | 0.001 | 0 | 0 |
| Diseases associated with glycosaminoglycan metabolism | R-HSA-3560782 | 9.984429e-01 | 0.001 | 0 | 0 |
| Ion transport by P-type ATPases | R-HSA-936837 | 9.985034e-01 | 0.001 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 9.987182e-01 | 0.001 | 0 | 0 |
| Carboxyterminal post-translational modifications of tubulin | R-HSA-8955332 | 9.987805e-01 | 0.001 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 9.988079e-01 | 0.001 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 9.988286e-01 | 0.001 | 0 | 0 |
| Ion channel transport | R-HSA-983712 | 9.988965e-01 | 0.000 | 0 | 0 |
| Intraflagellar transport | R-HSA-5620924 | 9.989207e-01 | 0.000 | 0 | 0 |
| Nicotinate metabolism | R-HSA-196807 | 9.989242e-01 | 0.000 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 9.989521e-01 | 0.000 | 0 | 0 |
| Peroxisomal lipid metabolism | R-HSA-390918 | 9.990010e-01 | 0.000 | 0 | 0 |
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | R-HSA-532668 | 9.990449e-01 | 0.000 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 9.990752e-01 | 0.000 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 9.990922e-01 | 0.000 | 0 | 0 |
| Hedgehog ligand biogenesis | R-HSA-5358346 | 9.992520e-01 | 0.000 | 0 | 0 |
| Diseases associated with O-glycosylation of proteins | R-HSA-3906995 | 9.993087e-01 | 0.000 | 0 | 0 |
| Metabolism of porphyrins | R-HSA-189445 | 9.993087e-01 | 0.000 | 0 | 0 |
| Hedgehog 'off' state | R-HSA-5610787 | 9.993227e-01 | 0.000 | 0 | 0 |
| Pyruvate metabolism | R-HSA-70268 | 9.993381e-01 | 0.000 | 0 | 0 |
| Beta-catenin independent WNT signaling | R-HSA-3858494 | 9.993551e-01 | 0.000 | 0 | 0 |
| Interconversion of nucleotide di- and triphosphates | R-HSA-499943 | 9.993813e-01 | 0.000 | 0 | 0 |
| Developmental Lineages of the Mammary Gland | R-HSA-9924644 | 9.993813e-01 | 0.000 | 0 | 0 |
| Interleukin-1 signaling | R-HSA-9020702 | 9.993857e-01 | 0.000 | 0 | 0 |
| Diseases of carbohydrate metabolism | R-HSA-5663084 | 9.994463e-01 | 0.000 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 9.994572e-01 | 0.000 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 9.994762e-01 | 0.000 | 0 | 0 |
| Glucuronidation | R-HSA-156588 | 9.994816e-01 | 0.000 | 0 | 0 |
| ROS and RNS production in phagocytes | R-HSA-1222556 | 9.995046e-01 | 0.000 | 0 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 9.995356e-01 | 0.000 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 9.995768e-01 | 0.000 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 9.995858e-01 | 0.000 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 9.996803e-01 | 0.000 | 0 | 0 |
| PCP/CE pathway | R-HSA-4086400 | 9.996829e-01 | 0.000 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 9.996829e-01 | 0.000 | 0 | 0 |
| Degradation of the extracellular matrix | R-HSA-1474228 | 9.996954e-01 | 0.000 | 0 | 0 |
| Heparan sulfate/heparin (HS-GAG) metabolism | R-HSA-1638091 | 9.997187e-01 | 0.000 | 0 | 0 |
| Sialic acid metabolism | R-HSA-4085001 | 9.997187e-01 | 0.000 | 0 | 0 |
| RAB geranylgeranylation | R-HSA-8873719 | 9.997511e-01 | 0.000 | 0 | 0 |
| GABA receptor activation | R-HSA-977443 | 9.997511e-01 | 0.000 | 0 | 0 |
| Sphingolipid de novo biosynthesis | R-HSA-1660661 | 9.997511e-01 | 0.000 | 0 | 0 |
| tRNA Aminoacylation | R-HSA-379724 | 9.997511e-01 | 0.000 | 0 | 0 |
| Amyloid fiber formation | R-HSA-977225 | 9.997733e-01 | 0.000 | 0 | 0 |
| Endogenous sterols | R-HSA-211976 | 9.997798e-01 | 0.000 | 0 | 0 |
| Role of LAT2/NTAL/LAB on calcium mobilization | R-HSA-2730905 | 9.997898e-01 | 0.000 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 9.998125e-01 | 0.000 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 9.998137e-01 | 0.000 | 0 | 0 |
| TNFR2 non-canonical NF-kB pathway | R-HSA-5668541 | 9.998189e-01 | 0.000 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 9.998452e-01 | 0.000 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 9.998549e-01 | 0.000 | 0 | 0 |
| Sulfur amino acid metabolism | R-HSA-1614635 | 9.998845e-01 | 0.000 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 9.998866e-01 | 0.000 | 0 | 0 |
| Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol | R-HSA-193368 | 9.998943e-01 | 0.000 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 9.999005e-01 | 0.000 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 9.999119e-01 | 0.000 | 1 | 0 |
| Cardiac conduction | R-HSA-5576891 | 9.999135e-01 | 0.000 | 0 | 0 |
| Interferon gamma signaling | R-HSA-877300 | 9.999228e-01 | 0.000 | 0 | 0 |
| Downstream TCR signaling | R-HSA-202424 | 9.999265e-01 | 0.000 | 0 | 0 |
| ECM proteoglycans | R-HSA-3000178 | 9.999352e-01 | 0.000 | 0 | 0 |
| Retinoid metabolism and transport | R-HSA-975634 | 9.999352e-01 | 0.000 | 0 | 0 |
| Metabolism of cofactors | R-HSA-8978934 | 9.999352e-01 | 0.000 | 0 | 0 |
| Transmission across Chemical Synapses | R-HSA-112315 | 9.999424e-01 | 0.000 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 9.999446e-01 | 0.000 | 0 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 9.999482e-01 | 0.000 | 0 | 0 |
| Citric acid cycle (TCA cycle) | R-HSA-71403 | 9.999603e-01 | 0.000 | 0 | 0 |
| Interleukin-10 signaling | R-HSA-6783783 | 9.999725e-01 | 0.000 | 0 | 0 |
| ABC transporter disorders | R-HSA-5619084 | 9.999725e-01 | 0.000 | 0 | 0 |
| Metabolic disorders of biological oxidation enzymes | R-HSA-5579029 | 9.999757e-01 | 0.000 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 9.999764e-01 | 0.000 | 0 | 0 |
| G alpha (s) signalling events | R-HSA-418555 | 9.999766e-01 | 0.000 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 9.999778e-01 | 0.000 | 0 | 0 |
| Synthesis of bile acids and bile salts | R-HSA-192105 | 9.999789e-01 | 0.000 | 0 | 0 |
| Metabolism of fat-soluble vitamins | R-HSA-6806667 | 9.999809e-01 | 0.000 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 9.999876e-01 | 0.000 | 0 | 0 |
| Disorders of transmembrane transporters | R-HSA-5619115 | 9.999893e-01 | 0.000 | 0 | 0 |
| Infection with Mycobacterium tuberculosis | R-HSA-9635486 | 9.999895e-01 | 0.000 | 0 | 0 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | R-HSA-163841 | 9.999909e-01 | 0.000 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 9.999916e-01 | 0.000 | 0 | 0 |
| Formation of the cornified envelope | R-HSA-6809371 | 9.999924e-01 | 0.000 | 0 | 0 |
| Antigen processing-Cross presentation | R-HSA-1236975 | 9.999933e-01 | 0.000 | 0 | 0 |
| ER-Phagosome pathway | R-HSA-1236974 | 9.999937e-01 | 0.000 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 9.999943e-01 | 0.000 | 0 | 0 |
| Class B/2 (Secretin family receptors) | R-HSA-373080 | 9.999944e-01 | 0.000 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 9.999945e-01 | 0.000 | 0 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 9.999945e-01 | 0.000 | 0 | 0 |
| Leishmania infection | R-HSA-9658195 | 9.999945e-01 | 0.000 | 0 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 9.999946e-01 | 0.000 | 0 | 0 |
| Bile acid and bile salt metabolism | R-HSA-194068 | 9.999947e-01 | 0.000 | 0 | 0 |
| Antimicrobial peptides | R-HSA-6803157 | 9.999953e-01 | 0.000 | 0 | 0 |
| Metabolism of steroids | R-HSA-8957322 | 9.999963e-01 | 0.000 | 0 | 0 |
| FCGR activation | R-HSA-2029481 | 9.999966e-01 | 0.000 | 0 | 0 |
| Mitochondrial protein degradation | R-HSA-9837999 | 9.999970e-01 | 0.000 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 9.999970e-01 | 0.000 | 0 | 0 |
| Mitochondrial Fatty Acid Beta-Oxidation | R-HSA-77289 | 9.999973e-01 | 0.000 | 0 | 0 |
| Role of phospholipids in phagocytosis | R-HSA-2029485 | 9.999976e-01 | 0.000 | 0 | 0 |
| Mitochondrial translation elongation | R-HSA-5389840 | 9.999979e-01 | 0.000 | 0 | 0 |
| Mitochondrial translation initiation | R-HSA-5368286 | 9.999984e-01 | 0.000 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 9.999984e-01 | 0.000 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 9.999987e-01 | 0.000 | 0 | 0 |
| Metabolism of water-soluble vitamins and cofactors | R-HSA-196849 | 9.999987e-01 | 0.000 | 0 | 0 |
| ABC-family proteins mediated transport | R-HSA-382556 | 9.999987e-01 | 0.000 | 0 | 0 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 9.999991e-01 | 0.000 | 0 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 9.999991e-01 | 0.000 | 0 | 0 |
| Mitochondrial ribosome-associated quality control | R-HSA-9937383 | 9.999991e-01 | 0.000 | 0 | 0 |
| Metabolism of nucleotides | R-HSA-15869 | 9.999993e-01 | 0.000 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 9.999993e-01 | 0.000 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 9.999995e-01 | 0.000 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 9.999995e-01 | 0.000 | 0 | 0 |
| Mitochondrial translation termination | R-HSA-5419276 | 9.999996e-01 | 0.000 | 0 | 0 |
| Synthesis of substrates in N-glycan biosythesis | R-HSA-446219 | 9.999997e-01 | 0.000 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 9.999998e-01 | 0.000 | 0 | 0 |
| SLC-mediated transmembrane transport | R-HSA-425407 | 9.999998e-01 | 0.000 | 0 | 0 |
| Peptide hormone metabolism | R-HSA-2980736 | 9.999999e-01 | 0.000 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 9.999999e-01 | 0.000 | 0 | 0 |
| G alpha (q) signalling events | R-HSA-416476 | 9.999999e-01 | 0.000 | 0 | 0 |
| Phase II - Conjugation of compounds | R-HSA-156580 | 1.000000e+00 | 0.000 | 0 | 0 |
| Binding and Uptake of Ligands by Scavenger Receptors | R-HSA-2173782 | 1.000000e+00 | 0.000 | 0 | 0 |
| Nucleotide catabolism | R-HSA-8956319 | 1.000000e+00 | 0.000 | 0 | 0 |
| Sensory perception of taste | R-HSA-9717189 | 1.000000e+00 | 0.000 | 0 | 0 |
| Translation | R-HSA-72766 | 1.000000e+00 | 0.000 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 1.000000e+00 | 0.000 | 1 | 0 |
| Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein | R-HSA-446193 | 1.000000e+00 | 0.000 | 0 | 0 |
| O-linked glycosylation | R-HSA-5173105 | 1.000000e+00 | 0.000 | 0 | 0 |
| Mitochondrial translation | R-HSA-5368287 | 1.000000e+00 | 0.000 | 0 | 0 |
| Diseases of glycosylation | R-HSA-3781865 | 1.000000e+00 | 0.000 | 0 | 0 |
| FCERI mediated NF-kB activation | R-HSA-2871837 | 1.000000e+00 | 0.000 | 0 | 0 |
| Glycosaminoglycan metabolism | R-HSA-1630316 | 1.000000e+00 | 0.000 | 0 | 0 |
| Visual phototransduction | R-HSA-2187338 | 1.000000e+00 | 0.000 | 0 | 0 |
| Arachidonate metabolism | R-HSA-2142753 | 1.000000e+00 | 0.000 | 0 | 0 |
| Respiratory electron transport | R-HSA-611105 | 1.000000e+00 | 0.000 | 0 | 0 |
| Keratinization | R-HSA-6805567 | 1.000000e+00 | 0.000 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 1.000000e+00 | 0.000 | 0 | 0 |
| Cytochrome P450 - arranged by substrate type | R-HSA-211897 | 1.000000e+00 | 0.000 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 1.000000e+00 | 0.000 | 0 | 0 |
| Metabolism of vitamins and cofactors | R-HSA-196854 | 1.000000e+00 | 0.000 | 0 | 0 |
| Sphingolipid metabolism | R-HSA-428157 | 1.000000e+00 | 0.000 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 1.000000e+00 | 0.000 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 1.000000e+00 | 0.000 | 0 | 0 |
| Metabolism of carbohydrates and carbohydrate derivatives | R-HSA-71387 | 1.000000e+00 | 0.000 | 0 | 0 |
| Fatty acid metabolism | R-HSA-8978868 | 1.000000e+00 | 0.000 | 0 | 0 |
| Disease | R-HSA-1643685 | 1.000000e+00 | 0.000 | 0 | 0 |
| G alpha (i) signalling events | R-HSA-418594 | 1.000000e+00 | 0.000 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 1.000000e+00 | 0.000 | 0 | 0 |
| Aerobic respiration and respiratory electron transport | R-HSA-1428517 | 1.000000e+00 | 0.000 | 0 | 0 |
| Immune System | R-HSA-168256 | 1.000000e+00 | 0.000 | 1 | 0 |
| Infectious disease | R-HSA-5663205 | 1.000000e+00 | 0.000 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 1.000000e+00 | 0.000 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 1.000000e+00 | 0.000 | 0 | 0 |
| Phase I - Functionalization of compounds | R-HSA-211945 | 1.000000e+00 | 0.000 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 1.000000e+00 | -0.000 | 1 | 0 |
| Metabolism of lipids | R-HSA-556833 | 1.000000e+00 | -0.000 | 0 | 0 |
| Olfactory Signaling Pathway | R-HSA-381753 | 1.000000e+00 | -0.000 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 1.000000e+00 | -0.000 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 1.000000e+00 | -0.000 | 0 | 0 |
| Diseases of metabolism | R-HSA-5668914 | 1.000000e+00 | -0.000 | 0 | 0 |
| Class A/1 (Rhodopsin-like receptors) | R-HSA-373076 | 1.000000e+00 | -0.000 | 0 | 0 |
| GPCR ligand binding | R-HSA-500792 | 1.000000e+00 | -0.000 | 0 | 0 |
| Biological oxidations | R-HSA-211859 | 1.000000e+00 | -0.000 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 1.000000e+00 | -0.000 | 0 | 0 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | R-HSA-8852276 | 1.000000e+00 | 0.000 | 1 | 1 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
Motif of predicted substrate sequence
Reactome pathways of predicted substrates
Download
| name | reactome_id | p | -log10p | ref_path | ref_path_lowest |
|---|---|---|---|---|---|
| Cell Cycle, Mitotic | R-HSA-69278 | 1.872540e-10 | 9.728 | 1 | 0 |
| Chromatin organization | R-HSA-4839726 | 1.603037e-09 | 8.795 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 3.147583e-09 | 8.502 | 1 | 0 |
| Formation of Senescence-Associated Heterochromatin Foci (SAHF) | R-HSA-2559584 | 4.356619e-08 | 7.361 | 0 | 0 |
| Chromatin modifying enzymes | R-HSA-3247509 | 4.445466e-08 | 7.352 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 7.405003e-07 | 6.130 | 0 | 0 |
| Apoptotic execution phase | R-HSA-75153 | 1.693033e-06 | 5.771 | 0 | 0 |
| M Phase | R-HSA-68886 | 3.916601e-06 | 5.407 | 1 | 0 |
| Formation of WDR5-containing histone-modifying complexes | R-HSA-9772755 | 9.848839e-06 | 5.007 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 1.762966e-05 | 4.754 | 0 | 0 |
| Formation of the beta-catenin:TCF transactivating complex | R-HSA-201722 | 1.980680e-05 | 4.703 | 0 | 0 |
| Mitotic Spindle Checkpoint | R-HSA-69618 | 4.212494e-05 | 4.375 | 0 | 0 |
| Signaling by high-kinase activity BRAF mutants | R-HSA-6802948 | 7.082160e-05 | 4.150 | 0 | 0 |
| Signaling by BRAF and RAF1 fusions | R-HSA-6802952 | 6.419281e-05 | 4.193 | 0 | 0 |
| ATP-dependent chromatin remodelers | R-HSA-9932444 | 7.280380e-05 | 4.138 | 0 | 0 |
| SWI/SNF chromatin remodelers | R-HSA-9932451 | 7.280380e-05 | 4.138 | 0 | 0 |
| Signal Transduction | R-HSA-162582 | 6.594504e-05 | 4.181 | 1 | 0 |
| Apoptotic cleavage of cellular proteins | R-HSA-111465 | 8.369545e-05 | 4.077 | 0 | 0 |
| Signaling by moderate kinase activity BRAF mutants | R-HSA-6802946 | 1.231729e-04 | 3.909 | 0 | 0 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | R-HSA-6802955 | 1.231729e-04 | 3.909 | 0 | 0 |
| Signaling downstream of RAS mutants | R-HSA-9649948 | 1.231729e-04 | 3.909 | 0 | 0 |
| Signaling by RAS mutants | R-HSA-6802949 | 1.231729e-04 | 3.909 | 0 | 0 |
| HIV Life Cycle | R-HSA-162587 | 1.150711e-04 | 3.939 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 1.092020e-04 | 3.962 | 0 | 0 |
| Interactions of Rev with host cellular proteins | R-HSA-177243 | 1.300250e-04 | 3.886 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 1.333343e-04 | 3.875 | 1 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 1.438201e-04 | 3.842 | 1 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 1.562524e-04 | 3.806 | 0 | 0 |
| Nuclear import of Rev protein | R-HSA-180746 | 1.608156e-04 | 3.794 | 0 | 0 |
| Regulation of TP53 Expression | R-HSA-6804754 | 1.866096e-04 | 3.729 | 0 | 0 |
| MAP2K and MAPK activation | R-HSA-5674135 | 1.896784e-04 | 3.722 | 0 | 0 |
| Signaling by RAF1 mutants | R-HSA-9656223 | 1.896784e-04 | 3.722 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 2.400190e-04 | 3.620 | 0 | 0 |
| Oncogenic MAPK signaling | R-HSA-6802957 | 3.209754e-04 | 3.494 | 0 | 0 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | R-HSA-141444 | 3.617244e-04 | 3.442 | 0 | 0 |
| Amplification of signal from the kinetochores | R-HSA-141424 | 3.617244e-04 | 3.442 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 3.653013e-04 | 3.437 | 1 | 0 |
| Rev-mediated nuclear export of HIV RNA | R-HSA-165054 | 3.510916e-04 | 3.455 | 0 | 0 |
| Transcription of E2F targets under negative control by DREAM complex | R-HSA-1362277 | 3.955226e-04 | 3.403 | 0 | 0 |
| Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | R-HSA-9934037 | 3.955226e-04 | 3.403 | 0 | 0 |
| Formation of the embryonic stem cell BAF (esBAF) complex | R-HSA-9933946 | 3.968590e-04 | 3.401 | 0 | 0 |
| Late Phase of HIV Life Cycle | R-HSA-162599 | 3.983796e-04 | 3.400 | 0 | 0 |
| Transport of Mature mRNA Derived from an Intronless Transcript | R-HSA-159231 | 4.207771e-04 | 3.376 | 0 | 0 |
| TFAP2A acts as a transcriptional repressor during retinoic acid induced cell differentiation | R-HSA-8869496 | 4.389484e-04 | 3.358 | 0 | 0 |
| tRNA processing in the nucleus | R-HSA-6784531 | 4.432248e-04 | 3.353 | 0 | 0 |
| Transport of Mature mRNAs Derived from Intronless Transcripts | R-HSA-159234 | 5.016969e-04 | 3.300 | 0 | 0 |
| DNA Damage Recognition in GG-NER | R-HSA-5696394 | 5.408555e-04 | 3.267 | 0 | 0 |
| Transport of Mature Transcript to Cytoplasm | R-HSA-72202 | 6.354321e-04 | 3.197 | 0 | 0 |
| Activation of RAC1 | R-HSA-428540 | 6.704680e-04 | 3.174 | 0 | 0 |
| RUNX3 regulates WNT signaling | R-HSA-8951430 | 7.030026e-04 | 3.153 | 0 | 0 |
| Binding of TCF/LEF:CTNNB1 to target gene promoters | R-HSA-4411364 | 7.030026e-04 | 3.153 | 0 | 0 |
| Role of ABL in ROBO-SLIT signaling | R-HSA-428890 | 7.030026e-04 | 3.153 | 0 | 0 |
| Nuclear Envelope Breakdown | R-HSA-2980766 | 6.979615e-04 | 3.156 | 1 | 0 |
| HATs acetylate histones | R-HSA-3214847 | 7.765457e-04 | 3.110 | 0 | 0 |
| Global Genome Nucleotide Excision Repair (GG-NER) | R-HSA-5696399 | 7.979186e-04 | 3.098 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 8.237792e-04 | 3.084 | 1 | 0 |
| RUNX3 regulates NOTCH signaling | R-HSA-8941856 | 9.326865e-04 | 3.030 | 0 | 0 |
| Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) | R-HSA-5619107 | 1.007776e-03 | 2.997 | 0 | 0 |
| NOTCH3 Intracellular Domain Regulates Transcription | R-HSA-9013508 | 1.007776e-03 | 2.997 | 0 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 9.714527e-04 | 3.013 | 1 | 0 |
| Vpr-mediated nuclear import of PICs | R-HSA-180910 | 1.102962e-03 | 2.957 | 0 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 1.060204e-03 | 2.975 | 0 | 0 |
| Deactivation of the beta-catenin transactivating complex | R-HSA-3769402 | 1.102962e-03 | 2.957 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 1.094250e-03 | 2.961 | 1 | 0 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | R-HSA-8864260 | 1.126914e-03 | 2.948 | 0 | 0 |
| IP3 and IP4 transport between cytosol and nucleus | R-HSA-1855196 | 1.215092e-03 | 2.915 | 0 | 0 |
| IP6 and IP7 transport between cytosol and nucleus | R-HSA-1855229 | 1.215092e-03 | 2.915 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 1.232808e-03 | 2.909 | 1 | 1 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 1.248731e-03 | 2.904 | 1 | 0 |
| Formation of the non-canonical BAF (ncBAF) complex | R-HSA-9933947 | 1.267447e-03 | 2.897 | 0 | 0 |
| DNA Damage/Telomere Stress Induced Senescence | R-HSA-2559586 | 1.346999e-03 | 2.871 | 0 | 0 |
| Expression of BMAL (ARNTL), CLOCK, and NPAS2 | R-HSA-9931509 | 1.525812e-03 | 2.816 | 0 | 0 |
| NS1 Mediated Effects on Host Pathways | R-HSA-168276 | 1.525812e-03 | 2.816 | 0 | 0 |
| HDMs demethylate histones | R-HSA-3214842 | 1.552084e-03 | 2.809 | 0 | 0 |
| Caspase-mediated cleavage of cytoskeletal proteins | R-HSA-264870 | 1.564970e-03 | 2.805 | 0 | 0 |
| IPs transport between nucleus and cytosol | R-HSA-1855170 | 1.732787e-03 | 2.761 | 0 | 0 |
| Transport of the SLBP independent Mature mRNA | R-HSA-159227 | 1.732787e-03 | 2.761 | 0 | 0 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | R-HSA-159236 | 1.739225e-03 | 2.760 | 0 | 0 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | R-HSA-8939243 | 1.732787e-03 | 2.761 | 0 | 0 |
| Formation of the canonical BAF (cBAF) complex | R-HSA-9933937 | 1.687049e-03 | 2.773 | 0 | 0 |
| Interactions of Vpr with host cellular proteins | R-HSA-176033 | 1.781866e-03 | 2.749 | 0 | 0 |
| Formation of the polybromo-BAF (pBAF) complex | R-HSA-9933939 | 1.687049e-03 | 2.773 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 1.873774e-03 | 2.727 | 0 | 0 |
| Transport of the SLBP Dependant Mature mRNA | R-HSA-159230 | 2.050792e-03 | 2.688 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 2.177978e-03 | 2.662 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 2.151229e-03 | 2.667 | 0 | 0 |
| TP53 Regulates Transcription of Cell Cycle Genes | R-HSA-6791312 | 2.124044e-03 | 2.673 | 1 | 0 |
| Regulation of Glucokinase by Glucokinase Regulatory Protein | R-HSA-170822 | 2.050792e-03 | 2.688 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 2.193493e-03 | 2.659 | 0 | 0 |
| Cell-extracellular matrix interactions | R-HSA-446353 | 2.204482e-03 | 2.657 | 0 | 0 |
| Apoptosis induced DNA fragmentation | R-HSA-140342 | 2.209044e-03 | 2.656 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 2.294542e-03 | 2.639 | 0 | 0 |
| UCH proteinases | R-HSA-5689603 | 2.407915e-03 | 2.618 | 0 | 0 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | R-HSA-9687136 | 2.833308e-03 | 2.548 | 0 | 0 |
| Nuclear Pore Complex (NPC) Disassembly | R-HSA-3301854 | 2.825720e-03 | 2.549 | 1 | 1 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 3.042259e-03 | 2.517 | 1 | 1 |
| S Phase | R-HSA-69242 | 3.082826e-03 | 2.511 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 3.175845e-03 | 2.498 | 1 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 3.444625e-03 | 2.463 | 1 | 0 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | R-HSA-141405 | 3.587529e-03 | 2.445 | 0 | 0 |
| Inactivation of APC/C via direct inhibition of the APC/C complex | R-HSA-141430 | 3.587529e-03 | 2.445 | 0 | 0 |
| Nucleotide Excision Repair | R-HSA-5696398 | 3.586025e-03 | 2.445 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 4.041249e-03 | 2.393 | 0 | 0 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | R-HSA-176407 | 4.481452e-03 | 2.349 | 0 | 0 |
| Signaling by Hippo | R-HSA-2028269 | 4.481452e-03 | 2.349 | 0 | 0 |
| Specification of primordial germ cells | R-HSA-9827857 | 4.481452e-03 | 2.349 | 0 | 0 |
| NOTCH2 intracellular domain regulates transcription | R-HSA-2197563 | 5.284738e-03 | 2.277 | 0 | 0 |
| Repression of WNT target genes | R-HSA-4641265 | 5.284738e-03 | 2.277 | 0 | 0 |
| RNA Polymerase II Pre-transcription Events | R-HSA-674695 | 5.072629e-03 | 2.295 | 0 | 0 |
| Signaling by ALK | R-HSA-201556 | 5.058133e-03 | 2.296 | 0 | 0 |
| Signaling by EGFR | R-HSA-177929 | 5.369879e-03 | 2.270 | 0 | 0 |
| TGFBR3 expression | R-HSA-9839394 | 6.095999e-03 | 2.215 | 0 | 0 |
| NFE2L2 regulating tumorigenic genes | R-HSA-9818030 | 6.772349e-03 | 2.169 | 0 | 0 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | R-HSA-9659787 | 6.772349e-03 | 2.169 | 0 | 0 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | R-HSA-9661069 | 6.772349e-03 | 2.169 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 6.566804e-03 | 2.183 | 0 | 0 |
| Regulation of TP53 Activity through Association with Co-factors | R-HSA-6804759 | 6.772349e-03 | 2.169 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 6.765762e-03 | 2.170 | 1 | 0 |
| PKMTs methylate histone lysines | R-HSA-3214841 | 6.593640e-03 | 2.181 | 0 | 0 |
| Transcriptional Regulation by VENTX | R-HSA-8853884 | 6.593640e-03 | 2.181 | 0 | 0 |
| Transport of Ribonucleoproteins into the Host Nucleus | R-HSA-168271 | 6.593640e-03 | 2.181 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 7.114616e-03 | 2.148 | 0 | 0 |
| Formation of annular gap junctions | R-HSA-196025 | 7.336343e-03 | 2.135 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in DNA replication, damage repair and senescence | R-HSA-9825895 | 7.336343e-03 | 2.135 | 0 | 0 |
| TP53 Regulates Transcription of DNA Repair Genes | R-HSA-6796648 | 7.392657e-03 | 2.131 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 7.637215e-03 | 2.117 | 0 | 0 |
| Diseases of Telomere Maintenance | R-HSA-9673013 | 8.532985e-03 | 2.069 | 0 | 0 |
| Alternative Lengthening of Telomeres (ALT) | R-HSA-9006821 | 8.532985e-03 | 2.069 | 0 | 0 |
| Defective Inhibition of DNA Recombination at Telomere | R-HSA-9670621 | 8.532985e-03 | 2.069 | 0 | 0 |
| Defective Inhibition of DNA Recombination at Telomere Due to DAXX Mutations | R-HSA-9670613 | 8.532985e-03 | 2.069 | 0 | 0 |
| Defective Inhibition of DNA Recombination at Telomere Due to ATRX Mutations | R-HSA-9670615 | 8.532985e-03 | 2.069 | 0 | 0 |
| RAF activation | R-HSA-5673000 | 8.096779e-03 | 2.092 | 0 | 0 |
| Regulation of PTEN gene transcription | R-HSA-8943724 | 8.232848e-03 | 2.084 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 9.094285e-03 | 2.041 | 0 | 0 |
| Viral Messenger RNA Synthesis | R-HSA-168325 | 9.106103e-03 | 2.041 | 0 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 9.280519e-03 | 2.032 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 9.280519e-03 | 2.032 | 0 | 0 |
| GP1b-IX-V activation signalling | R-HSA-430116 | 9.854005e-03 | 2.006 | 0 | 0 |
| Gap junction degradation | R-HSA-190873 | 9.854005e-03 | 2.006 | 0 | 0 |
| APC-Cdc20 mediated degradation of Nek2A | R-HSA-179409 | 9.743548e-03 | 2.011 | 0 | 0 |
| mRNA 3'-end processing | R-HSA-72187 | 9.438792e-03 | 2.025 | 0 | 0 |
| NOTCH4 Intracellular Domain Regulates Transcription | R-HSA-9013695 | 9.743548e-03 | 2.011 | 0 | 0 |
| DCC mediated attractive signaling | R-HSA-418885 | 1.058149e-02 | 1.975 | 0 | 0 |
| Axon guidance | R-HSA-422475 | 1.024611e-02 | 1.989 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 1.004920e-02 | 1.998 | 0 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 1.024571e-02 | 1.989 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 1.130133e-02 | 1.947 | 0 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 1.133987e-02 | 1.945 | 0 | 0 |
| Initiation of Nuclear Envelope (NE) Reformation | R-HSA-2995383 | 1.155196e-02 | 1.937 | 1 | 1 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 1.191776e-02 | 1.924 | 0 | 0 |
| NEP/NS2 Interacts with the Cellular Export Machinery | R-HSA-168333 | 1.199026e-02 | 1.921 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 1.204737e-02 | 1.919 | 0 | 0 |
| Oxidative Stress Induced Senescence | R-HSA-2559580 | 1.277747e-02 | 1.894 | 0 | 0 |
| Signaling by membrane-tethered fusions of PDGFRA or PDGFRB | R-HSA-9673768 | 1.279415e-02 | 1.893 | 0 | 0 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | R-HSA-1362300 | 1.294622e-02 | 1.888 | 1 | 1 |
| Activation of the pre-replicative complex | R-HSA-68962 | 1.303765e-02 | 1.885 | 0 | 0 |
| mTORC1-mediated signalling | R-HSA-166208 | 1.358493e-02 | 1.867 | 0 | 0 |
| TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain | R-HSA-6804115 | 1.358493e-02 | 1.867 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | R-HSA-6804116 | 1.294622e-02 | 1.888 | 0 | 0 |
| Regulation of PD-L1(CD274) transcription | R-HSA-9909649 | 1.458969e-02 | 1.836 | 0 | 0 |
| Signaling by NOTCH3 | R-HSA-9012852 | 1.287283e-02 | 1.890 | 0 | 0 |
| Positive Regulation of CDH1 Gene Transcription | R-HSA-9764790 | 1.287362e-02 | 1.890 | 0 | 0 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | R-HSA-210744 | 1.294622e-02 | 1.888 | 0 | 0 |
| Nervous system development | R-HSA-9675108 | 1.468636e-02 | 1.833 | 0 | 0 |
| ISG15 antiviral mechanism | R-HSA-1169408 | 1.347766e-02 | 1.870 | 0 | 0 |
| Export of Viral Ribonucleoproteins from Nucleus | R-HSA-168274 | 1.337962e-02 | 1.874 | 0 | 0 |
| Processing of Intronless Pre-mRNAs | R-HSA-77595 | 1.564417e-02 | 1.806 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 1.669310e-02 | 1.777 | 0 | 0 |
| DNA strand elongation | R-HSA-69190 | 1.698364e-02 | 1.770 | 0 | 0 |
| RNA Polymerase II Transcription Pre-Initiation And Promoter Opening | R-HSA-73779 | 1.705208e-02 | 1.768 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 1.724384e-02 | 1.763 | 0 | 0 |
| Transcription of the HIV genome | R-HSA-167172 | 1.736972e-02 | 1.760 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 1.736972e-02 | 1.760 | 0 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 1.739713e-02 | 1.760 | 0 | 0 |
| Negative feedback regulation of MAPK pathway | R-HSA-5674499 | 1.817029e-02 | 1.741 | 0 | 0 |
| NOTCH1 Intracellular Domain Regulates Transcription | R-HSA-2122947 | 1.826386e-02 | 1.738 | 0 | 0 |
| Breakdown of the nuclear lamina | R-HSA-352238 | 1.835716e-02 | 1.736 | 0 | 0 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 1.885952e-02 | 1.724 | 0 | 0 |
| Nuclear Envelope (NE) Reassembly | R-HSA-2995410 | 2.016155e-02 | 1.695 | 1 | 0 |
| Signaling by MET | R-HSA-6806834 | 2.016155e-02 | 1.695 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 2.052652e-02 | 1.688 | 0 | 0 |
| Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | R-HSA-9845323 | 2.057124e-02 | 1.687 | 0 | 0 |
| RNA Polymerase II HIV Promoter Escape | R-HSA-167162 | 2.120567e-02 | 1.674 | 0 | 0 |
| HIV Transcription Initiation | R-HSA-167161 | 2.120567e-02 | 1.674 | 0 | 0 |
| RNA Polymerase II Transcription Initiation | R-HSA-75953 | 2.120567e-02 | 1.674 | 0 | 0 |
| Postmitotic nuclear pore complex (NPC) reformation | R-HSA-9615933 | 2.420815e-02 | 1.616 | 0 | 0 |
| MTOR signalling | R-HSA-165159 | 2.353064e-02 | 1.628 | 0 | 0 |
| Regulation of NFE2L2 gene expression | R-HSA-9818749 | 2.461932e-02 | 1.609 | 0 | 0 |
| RNA Polymerase II Transcription Termination | R-HSA-73856 | 2.244471e-02 | 1.649 | 0 | 0 |
| Heme signaling | R-HSA-9707616 | 2.443879e-02 | 1.612 | 0 | 0 |
| Transcriptional regulation by small RNAs | R-HSA-5578749 | 2.408699e-02 | 1.618 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 2.273665e-02 | 1.643 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 2.463223e-02 | 1.608 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Cyclin B | R-HSA-174048 | 2.590591e-02 | 1.587 | 1 | 1 |
| RNA Polymerase II Promoter Escape | R-HSA-73776 | 2.602896e-02 | 1.585 | 0 | 0 |
| Regulation of HSF1-mediated heat shock response | R-HSA-3371453 | 2.628482e-02 | 1.580 | 0 | 0 |
| Inositol phosphate metabolism | R-HSA-1483249 | 2.640289e-02 | 1.578 | 0 | 0 |
| Signalling to ERKs | R-HSA-187687 | 2.726707e-02 | 1.564 | 0 | 0 |
| Netrin-1 signaling | R-HSA-373752 | 2.870616e-02 | 1.542 | 0 | 0 |
| RUNX2 regulates bone development | R-HSA-8941326 | 3.038082e-02 | 1.517 | 0 | 0 |
| RET signaling | R-HSA-8853659 | 3.038082e-02 | 1.517 | 0 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 3.089350e-02 | 1.510 | 1 | 0 |
| RUNX2 regulates osteoblast differentiation | R-HSA-8940973 | 3.116467e-02 | 1.506 | 0 | 0 |
| Localization of the PINCH-ILK-PARVIN complex to focal adhesions | R-HSA-446343 | 3.121186e-02 | 1.506 | 0 | 0 |
| RNA Polymerase II Transcription Initiation And Promoter Clearance | R-HSA-76042 | 3.156749e-02 | 1.501 | 0 | 0 |
| Activation of HOX genes during differentiation | R-HSA-5619507 | 3.166853e-02 | 1.499 | 0 | 0 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | R-HSA-5617472 | 3.166853e-02 | 1.499 | 0 | 0 |
| SOS-mediated signalling | R-HSA-112412 | 3.214308e-02 | 1.493 | 0 | 0 |
| SHOC2 M1731 mutant abolishes MRAS complex function | R-HSA-9726840 | 3.214308e-02 | 1.493 | 0 | 0 |
| Activation of PUMA and translocation to mitochondria | R-HSA-139915 | 3.214308e-02 | 1.493 | 0 | 0 |
| Signaling by NOTCH1 | R-HSA-1980143 | 3.252128e-02 | 1.488 | 0 | 0 |
| RNA polymerase II transcribes snRNA genes | R-HSA-6807505 | 3.329055e-02 | 1.478 | 0 | 0 |
| Type I hemidesmosome assembly | R-HSA-446107 | 4.072752e-02 | 1.390 | 0 | 0 |
| Signaling by MRAS-complex mutants | R-HSA-9660537 | 4.072752e-02 | 1.390 | 0 | 0 |
| Gain-of-function MRAS complexes activate RAF signaling | R-HSA-9726842 | 4.072752e-02 | 1.390 | 0 | 0 |
| Processive synthesis on the lagging strand | R-HSA-69183 | 4.290309e-02 | 1.368 | 0 | 0 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | R-HSA-450513 | 4.290309e-02 | 1.368 | 0 | 0 |
| Gap-filling DNA repair synthesis and ligation in GG-NER | R-HSA-5696397 | 3.969238e-02 | 1.401 | 0 | 0 |
| RORA,B,C and NR1D1 (REV-ERBA) regulate gene expression | R-HSA-9933387 | 3.931006e-02 | 1.405 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 3.730542e-02 | 1.428 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 3.781297e-02 | 1.422 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 3.951079e-02 | 1.403 | 1 | 0 |
| STAT3 nuclear events downstream of ALK signaling | R-HSA-9701898 | 4.290309e-02 | 1.368 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 3.733549e-02 | 1.428 | 0 | 0 |
| Nuclear events stimulated by ALK signaling in cancer | R-HSA-9725371 | 4.130334e-02 | 1.384 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 4.017956e-02 | 1.396 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 3.913959e-02 | 1.407 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | R-HSA-9825892 | 3.969238e-02 | 1.401 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 4.016165e-02 | 1.396 | 0 | 0 |
| Deadenylation-dependent mRNA decay | R-HSA-429914 | 4.377557e-02 | 1.359 | 0 | 0 |
| snRNP Assembly | R-HSA-191859 | 4.377557e-02 | 1.359 | 0 | 0 |
| Metabolism of non-coding RNA | R-HSA-194441 | 4.377557e-02 | 1.359 | 0 | 0 |
| MET interacts with TNS proteins | R-HSA-8875513 | 4.665430e-02 | 1.331 | 0 | 0 |
| Positive epigenetic regulation of rRNA expression | R-HSA-5250913 | 4.839382e-02 | 1.315 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 4.923359e-02 | 1.308 | 0 | 0 |
| Resolution of Abasic Sites (AP sites) | R-HSA-73933 | 4.951096e-02 | 1.305 | 0 | 0 |
| Adipogenesis | R-HSA-9843745 | 4.971829e-02 | 1.303 | 0 | 0 |
| Phosphorylation of the APC/C | R-HSA-176412 | 5.001231e-02 | 1.301 | 1 | 1 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | R-HSA-354194 | 5.001231e-02 | 1.301 | 0 | 0 |
| Prolonged ERK activation events | R-HSA-169893 | 5.001231e-02 | 1.301 | 0 | 0 |
| Inactivation of CDC42 and RAC1 | R-HSA-428543 | 5.034546e-02 | 1.298 | 0 | 0 |
| ALK mutants bind TKIs | R-HSA-9700645 | 5.034546e-02 | 1.298 | 0 | 0 |
| Unwinding of DNA | R-HSA-176974 | 5.034546e-02 | 1.298 | 0 | 0 |
| Regulation of endogenous retroelements | R-HSA-9842860 | 5.087941e-02 | 1.293 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 5.217217e-02 | 1.283 | 0 | 0 |
| Defective translocation of RB1 mutants to the nucleus | R-HSA-9661070 | 6.608932e-02 | 1.180 | 0 | 0 |
| APC truncation mutants are not K63 polyubiquitinated | R-HSA-5467333 | 6.608932e-02 | 1.180 | 0 | 0 |
| Loss of function of TP53 in cancer due to loss of tetramerization ability | R-HSA-9723905 | 6.608932e-02 | 1.180 | 0 | 0 |
| Loss of Function of TP53 in Cancer | R-HSA-9723907 | 6.608932e-02 | 1.180 | 0 | 0 |
| Regulation of gap junction activity | R-HSA-191650 | 6.428694e-02 | 1.192 | 0 | 0 |
| Inhibition of TSC complex formation by PKB | R-HSA-165181 | 6.428694e-02 | 1.192 | 0 | 0 |
| NFE2L2 regulating ER-stress associated genes | R-HSA-9818035 | 6.428694e-02 | 1.192 | 0 | 0 |
| MET activates RAP1 and RAC1 | R-HSA-8875555 | 6.095909e-02 | 1.215 | 0 | 0 |
| The CRY:PER:kinase complex represses transactivation by the BMAL:CLOCK (ARNTL:CLOCK) complex | R-HSA-9931521 | 5.772752e-02 | 1.239 | 0 | 0 |
| mRNA decay by 5' to 3' exoribonuclease | R-HSA-430039 | 5.772752e-02 | 1.239 | 0 | 0 |
| p130Cas linkage to MAPK signaling for integrins | R-HSA-372708 | 6.604076e-02 | 1.180 | 0 | 0 |
| Deadenylation of mRNA | R-HSA-429947 | 5.721557e-02 | 1.242 | 0 | 0 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | R-HSA-174178 | 6.159311e-02 | 1.210 | 0 | 0 |
| Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) | R-HSA-5358565 | 6.604076e-02 | 1.180 | 0 | 0 |
| G1/S Transition | R-HSA-69206 | 6.222794e-02 | 1.206 | 1 | 0 |
| Integrin signaling | R-HSA-354192 | 5.385883e-02 | 1.269 | 0 | 0 |
| Activation of NOXA and translocation to mitochondria | R-HSA-111448 | 6.428694e-02 | 1.192 | 0 | 0 |
| Signal attenuation | R-HSA-74749 | 6.095909e-02 | 1.215 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 5.531741e-02 | 1.257 | 0 | 0 |
| Activation of ATR in response to replication stress | R-HSA-176187 | 5.385883e-02 | 1.269 | 0 | 0 |
| Negative regulation of MAPK pathway | R-HSA-5675221 | 5.408018e-02 | 1.267 | 0 | 0 |
| Transcriptional activation of cell cycle inhibitor p21 | R-HSA-69895 | 6.428694e-02 | 1.192 | 0 | 0 |
| Transcriptional activation of p53 responsive genes | R-HSA-69560 | 6.428694e-02 | 1.192 | 0 | 0 |
| Receptor Mediated Mitophagy | R-HSA-8934903 | 6.095909e-02 | 1.215 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | R-HSA-6804114 | 5.772752e-02 | 1.239 | 1 | 1 |
| Maternal to zygotic transition (MZT) | R-HSA-9816359 | 5.382218e-02 | 1.269 | 0 | 0 |
| Cargo recognition for clathrin-mediated endocytosis | R-HSA-8856825 | 5.675611e-02 | 1.246 | 0 | 0 |
| Processing of Capped Intronless Pre-mRNA | R-HSA-75067 | 5.721557e-02 | 1.242 | 0 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 6.436663e-02 | 1.191 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 6.570930e-02 | 1.182 | 0 | 0 |
| Host Interactions of HIV factors | R-HSA-162909 | 5.653167e-02 | 1.248 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 6.134399e-02 | 1.212 | 0 | 0 |
| Uptake and function of anthrax toxins | R-HSA-5210891 | 6.604076e-02 | 1.180 | 0 | 0 |
| Transcriptional regulation of white adipocyte differentiation | R-HSA-381340 | 6.826882e-02 | 1.166 | 0 | 0 |
| G1 Phase | R-HSA-69236 | 6.932400e-02 | 1.159 | 0 | 0 |
| Cyclin D associated events in G1 | R-HSA-69231 | 6.932400e-02 | 1.159 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 6.971306e-02 | 1.157 | 0 | 0 |
| Signaling by FLT3 fusion proteins | R-HSA-9703465 | 7.100277e-02 | 1.149 | 0 | 0 |
| Oncogene Induced Senescence | R-HSA-2559585 | 7.127783e-02 | 1.147 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 7.380384e-02 | 1.132 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 7.380384e-02 | 1.132 | 0 | 0 |
| Platelet Aggregation (Plug Formation) | R-HSA-76009 | 7.492088e-02 | 1.125 | 0 | 0 |
| Polo-like kinase mediated events | R-HSA-156711 | 7.494038e-02 | 1.125 | 0 | 0 |
| Mismatch Repair | R-HSA-5358508 | 7.494038e-02 | 1.125 | 0 | 0 |
| Depolymerization of the Nuclear Lamina | R-HSA-4419969 | 7.494038e-02 | 1.125 | 1 | 1 |
| Regulation of MITF-M-dependent genes involved in extracellular matrix, focal adhesion and epithelial-to-mesenchymal transition | R-HSA-9926550 | 7.494038e-02 | 1.125 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 7.707478e-02 | 1.113 | 0 | 0 |
| G1/S-Specific Transcription | R-HSA-69205 | 7.772469e-02 | 1.109 | 1 | 1 |
| RNA Polymerase III Abortive And Retractive Initiation | R-HSA-749476 | 7.772469e-02 | 1.109 | 0 | 0 |
| RNA Polymerase III Transcription | R-HSA-74158 | 7.772469e-02 | 1.109 | 0 | 0 |
| Interaction between L1 and Ankyrins | R-HSA-445095 | 7.852118e-02 | 1.105 | 0 | 0 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 8.375336e-02 | 1.077 | 0 | 0 |
| NFE2L2 regulating inflammation associated genes | R-HSA-9818026 | 8.375336e-02 | 1.077 | 0 | 0 |
| IRS activation | R-HSA-74713 | 8.375336e-02 | 1.077 | 0 | 0 |
| G2 Phase | R-HSA-68911 | 8.375336e-02 | 1.077 | 0 | 0 |
| RUNX3 regulates CDKN1A transcription | R-HSA-8941855 | 1.047347e-01 | 0.980 | 0 | 0 |
| Epithelial-Mesenchymal Transition (EMT) during gastrulation | R-HSA-9758919 | 1.047347e-01 | 0.980 | 0 | 0 |
| SLIT2:ROBO1 increases RHOA activity | R-HSA-8985586 | 1.047347e-01 | 0.980 | 0 | 0 |
| Phosphorylation of Emi1 | R-HSA-176417 | 1.047347e-01 | 0.980 | 1 | 1 |
| Inhibition of replication initiation of damaged DNA by RB1/E2F1 | R-HSA-113501 | 8.498158e-02 | 1.071 | 0 | 0 |
| Phosphorylation of CLOCK, acetylation of BMAL1 (ARNTL) at target gene promoters | R-HSA-9931512 | 8.498158e-02 | 1.071 | 0 | 0 |
| RUNX3 regulates p14-ARF | R-HSA-8951936 | 9.827960e-02 | 1.008 | 0 | 0 |
| Z-decay: degradation of maternal mRNAs by zygotically expressed factors | R-HSA-9820865 | 9.827960e-02 | 1.008 | 0 | 0 |
| Abortive elongation of HIV-1 transcript in the absence of Tat | R-HSA-167242 | 8.441137e-02 | 1.074 | 0 | 0 |
| Lagging Strand Synthesis | R-HSA-69186 | 1.049929e-01 | 0.979 | 0 | 0 |
| HIV elongation arrest and recovery | R-HSA-167287 | 8.644892e-02 | 1.063 | 0 | 0 |
| Pausing and recovery of HIV elongation | R-HSA-167290 | 8.644892e-02 | 1.063 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 9.694648e-02 | 1.013 | 1 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 9.694648e-02 | 1.013 | 1 | 0 |
| RNA Polymerase III Transcription Initiation | R-HSA-76046 | 1.035009e-01 | 0.985 | 0 | 0 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 8.229160e-02 | 1.085 | 1 | 1 |
| Recycling pathway of L1 | R-HSA-437239 | 8.688728e-02 | 1.061 | 0 | 0 |
| Resolution of AP sites via the single-nucleotide replacement pathway | R-HSA-110381 | 8.375336e-02 | 1.077 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 8.989195e-02 | 1.046 | 0 | 0 |
| PTK6 Regulates Proteins Involved in RNA Processing | R-HSA-8849468 | 8.375336e-02 | 1.077 | 0 | 0 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | R-HSA-2894862 | 9.894930e-02 | 1.005 | 0 | 0 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | R-HSA-2644602 | 9.894930e-02 | 1.005 | 0 | 0 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | R-HSA-2644606 | 9.894930e-02 | 1.005 | 0 | 0 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | R-HSA-2894858 | 9.894930e-02 | 1.005 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 8.918241e-02 | 1.050 | 0 | 0 |
| Assembly of the pre-replicative complex | R-HSA-68867 | 1.008683e-01 | 0.996 | 0 | 0 |
| Signaling by LTK | R-HSA-9842663 | 9.827960e-02 | 1.008 | 0 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 1.047395e-01 | 0.980 | 1 | 1 |
| Regulation of cytoskeletal remodeling and cell spreading by IPP complex components | R-HSA-446388 | 1.047347e-01 | 0.980 | 0 | 0 |
| MAP kinase activation | R-HSA-450294 | 1.051412e-01 | 0.978 | 0 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 9.443574e-02 | 1.025 | 0 | 0 |
| Zygotic genome activation (ZGA) | R-HSA-9819196 | 1.049929e-01 | 0.979 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 8.672062e-02 | 1.062 | 0 | 0 |
| RUNX1 regulates expression of components of tight junctions | R-HSA-8935964 | 1.047347e-01 | 0.980 | 0 | 0 |
| AKT phosphorylates targets in the cytosol | R-HSA-198323 | 9.827960e-02 | 1.008 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 9.971101e-02 | 1.001 | 0 | 0 |
| Signaling by NOTCH1 in Cancer | R-HSA-2644603 | 9.894930e-02 | 1.005 | 0 | 0 |
| NGF-stimulated transcription | R-HSA-9031628 | 9.325420e-02 | 1.030 | 0 | 0 |
| Nuclear Events (kinase and transcription factor activation) | R-HSA-198725 | 1.025692e-01 | 0.989 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 7.986314e-02 | 1.098 | 0 | 0 |
| LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production | R-HSA-3134973 | 8.375336e-02 | 1.077 | 0 | 0 |
| Interleukin-15 signaling | R-HSA-8983432 | 9.827960e-02 | 1.008 | 0 | 0 |
| Signaling by TGFBR3 | R-HSA-9839373 | 8.077563e-02 | 1.093 | 0 | 0 |
| Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | R-HSA-9851695 | 1.054257e-01 | 0.977 | 0 | 0 |
| MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis | R-HSA-9841922 | 1.054257e-01 | 0.977 | 0 | 0 |
| Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | R-HSA-9818564 | 1.054257e-01 | 0.977 | 0 | 0 |
| Signaling by VEGF | R-HSA-194138 | 1.054257e-01 | 0.977 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 1.066527e-01 | 0.972 | 0 | 0 |
| NR1H2 & NR1H3 regulate gene expression linked to lipogenesis | R-HSA-9029558 | 1.123547e-01 | 0.949 | 0 | 0 |
| Frs2-mediated activation | R-HSA-170968 | 1.123547e-01 | 0.949 | 0 | 0 |
| EGFR downregulation | R-HSA-182971 | 1.126056e-01 | 0.948 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 1.126056e-01 | 0.948 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 1.136599e-01 | 0.944 | 1 | 0 |
| M-decay: degradation of maternal mRNAs by maternally stored factors | R-HSA-9820841 | 1.146472e-01 | 0.941 | 0 | 0 |
| Signaling by PDGFR in disease | R-HSA-9671555 | 1.160598e-01 | 0.935 | 0 | 0 |
| FOXO-mediated transcription of cell cycle genes | R-HSA-9617828 | 1.160598e-01 | 0.935 | 0 | 0 |
| Activation of gene expression by SREBF (SREBP) | R-HSA-2426168 | 1.181511e-01 | 0.928 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 1.181511e-01 | 0.928 | 1 | 1 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 1.181511e-01 | 0.928 | 1 | 1 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 1.181511e-01 | 0.928 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 1.181511e-01 | 0.928 | 0 | 0 |
| Gene Silencing by RNA | R-HSA-211000 | 1.212084e-01 | 0.916 | 0 | 0 |
| Formation of RNA Pol II elongation complex | R-HSA-112382 | 1.212199e-01 | 0.916 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 1.215841e-01 | 0.915 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 1.220774e-01 | 0.913 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 1.245882e-01 | 0.905 | 1 | 0 |
| Developmental Cell Lineages of the Integumentary System | R-HSA-9734779 | 1.264506e-01 | 0.898 | 0 | 0 |
| RUNX3 regulates YAP1-mediated transcription | R-HSA-8951671 | 1.269460e-01 | 0.896 | 0 | 0 |
| CREB phosphorylation | R-HSA-199920 | 1.269460e-01 | 0.896 | 0 | 0 |
| Removal of the Flap Intermediate | R-HSA-69166 | 1.271429e-01 | 0.896 | 0 | 0 |
| Signal regulatory protein family interactions | R-HSA-391160 | 1.271429e-01 | 0.896 | 0 | 0 |
| Notch-HLH transcription pathway | R-HSA-350054 | 1.276116e-01 | 0.894 | 0 | 0 |
| TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain | R-HSA-6803205 | 1.276116e-01 | 0.894 | 0 | 0 |
| Regulation of PAK-2p34 activity by PS-GAP/RHG10 | R-HSA-211728 | 1.278145e-01 | 0.893 | 0 | 0 |
| Defective Mismatch Repair Associated With MSH6 | R-HSA-5632968 | 1.278145e-01 | 0.893 | 0 | 0 |
| RNA Polymerase II Transcription Elongation | R-HSA-75955 | 1.288169e-01 | 0.890 | 0 | 0 |
| B-WICH complex positively regulates rRNA expression | R-HSA-5250924 | 1.288169e-01 | 0.890 | 0 | 0 |
| Golgi Associated Vesicle Biogenesis | R-HSA-432722 | 1.288169e-01 | 0.890 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 1.315068e-01 | 0.881 | 0 | 0 |
| Nuclear RNA decay | R-HSA-9930044 | 1.319136e-01 | 0.880 | 0 | 0 |
| Regulation of TP53 Activity through Acetylation | R-HSA-6804758 | 1.319136e-01 | 0.880 | 0 | 0 |
| Synthesis of IP3 and IP4 in the cytosol | R-HSA-1855204 | 1.319136e-01 | 0.880 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 1.329590e-01 | 0.876 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 1.391872e-01 | 0.856 | 1 | 1 |
| Interleukin receptor SHC signaling | R-HSA-912526 | 1.396218e-01 | 0.855 | 0 | 0 |
| Estrogen-dependent nuclear events downstream of ESR-membrane signaling | R-HSA-9634638 | 1.396218e-01 | 0.855 | 0 | 0 |
| Constitutive Signaling by AKT1 E17K in Cancer | R-HSA-5674400 | 1.396218e-01 | 0.855 | 0 | 0 |
| Erythropoietin activates RAS | R-HSA-9027284 | 1.425792e-01 | 0.846 | 0 | 0 |
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | R-HSA-450385 | 1.425792e-01 | 0.846 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 1.447031e-01 | 0.840 | 1 | 0 |
| HDACs deacetylate histones | R-HSA-3214815 | 1.447031e-01 | 0.840 | 0 | 0 |
| Glycolysis | R-HSA-70171 | 1.448052e-01 | 0.839 | 0 | 0 |
| Defective VWF binding to collagen type I | R-HSA-9845622 | 1.854636e-01 | 0.732 | 0 | 0 |
| Signaling by TCF7L2 mutants | R-HSA-5339700 | 1.854636e-01 | 0.732 | 0 | 0 |
| Defective MMADHC causes MMAHCD | R-HSA-3359473 | 1.854636e-01 | 0.732 | 0 | 0 |
| NOSTRIN mediated eNOS trafficking | R-HSA-203641 | 1.501334e-01 | 0.824 | 0 | 0 |
| Cohesin Loading onto Chromatin | R-HSA-2470946 | 1.501334e-01 | 0.824 | 0 | 0 |
| NFE2L2 regulating MDR associated enzymes | R-HSA-9818032 | 1.985593e-01 | 0.702 | 0 | 0 |
| ARMS-mediated activation | R-HSA-170984 | 1.985593e-01 | 0.702 | 0 | 0 |
| Ephrin signaling | R-HSA-3928664 | 2.094978e-01 | 0.679 | 0 | 0 |
| PCNA-Dependent Long Patch Base Excision Repair | R-HSA-5651801 | 2.094978e-01 | 0.679 | 0 | 0 |
| Phosphorylated BMAL1:CLOCK (ARNTL:CLOCK) activates expression of core clock genes | R-HSA-9931510 | 1.781182e-01 | 0.749 | 0 | 0 |
| Tat-mediated HIV elongation arrest and recovery | R-HSA-167243 | 1.916732e-01 | 0.717 | 0 | 0 |
| Pausing and recovery of Tat-mediated HIV elongation | R-HSA-167238 | 1.916732e-01 | 0.717 | 0 | 0 |
| Formation of the HIV-1 Early Elongation Complex | R-HSA-167158 | 2.055388e-01 | 0.687 | 0 | 0 |
| Formation of the Early Elongation Complex | R-HSA-113418 | 2.055388e-01 | 0.687 | 0 | 0 |
| Developmental Lineage of Mammary Gland Myoepithelial Cells | R-HSA-9927432 | 2.196841e-01 | 0.658 | 0 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 1.529804e-01 | 0.815 | 1 | 0 |
| Gap-filling DNA repair synthesis and ligation in TC-NER | R-HSA-6782210 | 1.529804e-01 | 0.815 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Securin | R-HSA-174154 | 1.783332e-01 | 0.749 | 0 | 0 |
| Regulation of cholesterol biosynthesis by SREBP (SREBF) | R-HSA-1655829 | 1.469154e-01 | 0.833 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 2.068817e-01 | 0.684 | 1 | 1 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 1.947895e-01 | 0.710 | 1 | 1 |
| Centrosome maturation | R-HSA-380287 | 2.121614e-01 | 0.673 | 1 | 0 |
| PPARA activates gene expression | R-HSA-1989781 | 2.116436e-01 | 0.674 | 0 | 0 |
| Regulation of lipid metabolism by PPARalpha | R-HSA-400206 | 1.518816e-01 | 0.818 | 0 | 0 |
| Signaling by NOTCH2 | R-HSA-1980145 | 1.525949e-01 | 0.816 | 0 | 0 |
| HCMV Early Events | R-HSA-9609690 | 1.585233e-01 | 0.800 | 0 | 0 |
| Developmental Lineages of the Mammary Gland | R-HSA-9924644 | 1.863333e-01 | 0.730 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 1.494733e-01 | 0.825 | 0 | 0 |
| Recognition of DNA damage by PCNA-containing replication complex | R-HSA-110314 | 1.520625e-01 | 0.818 | 0 | 0 |
| TRAF3-dependent IRF activation pathway | R-HSA-918233 | 1.751331e-01 | 0.757 | 0 | 0 |
| GAB1 signalosome | R-HSA-180292 | 2.094978e-01 | 0.679 | 0 | 0 |
| Activated NTRK3 signals through PI3K | R-HSA-9603381 | 1.501334e-01 | 0.824 | 0 | 0 |
| BH3-only proteins associate with and inactivate anti-apoptotic BCL-2 members | R-HSA-111453 | 1.740713e-01 | 0.759 | 0 | 0 |
| Signaling by cytosolic FGFR1 fusion mutants | R-HSA-1839117 | 2.094978e-01 | 0.679 | 0 | 0 |
| Signaling by CSF1 (M-CSF) in myeloid cells | R-HSA-9680350 | 1.525949e-01 | 0.816 | 0 | 0 |
| Senescence-Associated Secretory Phenotype (SASP) | R-HSA-2559582 | 1.684505e-01 | 0.774 | 0 | 0 |
| Assembly of collagen fibrils and other multimeric structures | R-HSA-2022090 | 1.790687e-01 | 0.747 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 2.191263e-01 | 0.659 | 0 | 0 |
| Regulation of commissural axon pathfinding by SLIT and ROBO | R-HSA-428542 | 1.985593e-01 | 0.702 | 0 | 0 |
| APEX1-Independent Resolution of AP Sites via the Single Nucleotide Replacement Pathway | R-HSA-5649702 | 1.985593e-01 | 0.702 | 0 | 0 |
| trans-Golgi Network Vesicle Budding | R-HSA-199992 | 1.863333e-01 | 0.730 | 0 | 0 |
| Regulation of TP53 Expression and Degradation | R-HSA-6806003 | 2.094689e-01 | 0.679 | 1 | 0 |
| Defective Mismatch Repair Associated With MSH2 | R-HSA-5632928 | 1.854636e-01 | 0.732 | 0 | 0 |
| Inhibition of Host mRNA Processing and RNA Silencing | R-HSA-168315 | 1.854636e-01 | 0.732 | 0 | 0 |
| Disorders of Developmental Biology | R-HSA-9675151 | 1.751331e-01 | 0.757 | 0 | 0 |
| Serotonin Neurotransmitter Release Cycle | R-HSA-181429 | 2.094978e-01 | 0.679 | 0 | 0 |
| DNA Repair | R-HSA-73894 | 1.829491e-01 | 0.738 | 0 | 0 |
| Negative Regulation of CDH1 Gene Transcription | R-HSA-9764725 | 1.881588e-01 | 0.725 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 1.514240e-01 | 0.820 | 0 | 0 |
| CD209 (DC-SIGN) signaling | R-HSA-5621575 | 1.520625e-01 | 0.818 | 0 | 0 |
| Regulation of TNFR1 signaling | R-HSA-5357905 | 1.684723e-01 | 0.773 | 0 | 0 |
| FLT3 signaling in disease | R-HSA-9682385 | 1.745261e-01 | 0.758 | 0 | 0 |
| Interleukin-17 signaling | R-HSA-448424 | 1.699115e-01 | 0.770 | 0 | 0 |
| Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) | R-HSA-5358606 | 1.921209e-01 | 0.716 | 0 | 0 |
| SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription | R-HSA-2173796 | 1.859186e-01 | 0.731 | 0 | 0 |
| Gap junction trafficking and regulation | R-HSA-157858 | 1.987221e-01 | 0.702 | 0 | 0 |
| MAPK targets/ Nuclear events mediated by MAP kinases | R-HSA-450282 | 2.196841e-01 | 0.658 | 0 | 0 |
| Protein-protein interactions at synapses | R-HSA-6794362 | 1.913649e-01 | 0.718 | 0 | 0 |
| Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | R-HSA-2173793 | 1.529804e-01 | 0.815 | 0 | 0 |
| Displacement of DNA glycosylase by APEX1 | R-HSA-110357 | 1.501334e-01 | 0.824 | 0 | 0 |
| Activation of the TFAP2 (AP-2) family of transcription factors | R-HSA-8866907 | 1.985593e-01 | 0.702 | 0 | 0 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | R-HSA-9705671 | 2.122005e-01 | 0.673 | 0 | 0 |
| Transcriptional activation of mitochondrial biogenesis | R-HSA-2151201 | 1.611134e-01 | 0.793 | 0 | 0 |
| Regulation of CDH11 gene transcription | R-HSA-9762293 | 1.985593e-01 | 0.702 | 0 | 0 |
| Apoptotic cleavage of cell adhesion proteins | R-HSA-351906 | 1.740713e-01 | 0.759 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in pigmentation | R-HSA-9824585 | 1.588487e-01 | 0.799 | 0 | 0 |
| Receptor-type tyrosine-protein phosphatases | R-HSA-388844 | 1.585977e-01 | 0.800 | 0 | 0 |
| TFAP2 (AP-2) family regulates transcription of growth factors and their receptors | R-HSA-8866910 | 1.751331e-01 | 0.757 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 1.529804e-01 | 0.815 | 0 | 0 |
| Formation of HIV elongation complex in the absence of HIV Tat | R-HSA-167152 | 2.215902e-01 | 0.654 | 0 | 0 |
| Formation of Incision Complex in GG-NER | R-HSA-5696395 | 2.215902e-01 | 0.654 | 0 | 0 |
| Establishment of Sister Chromatid Cohesion | R-HSA-2468052 | 2.234205e-01 | 0.651 | 0 | 0 |
| PI3K/AKT activation | R-HSA-198203 | 2.234205e-01 | 0.651 | 0 | 0 |
| EGFR Transactivation by Gastrin | R-HSA-2179392 | 2.234205e-01 | 0.651 | 0 | 0 |
| Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RNA | R-HSA-428359 | 2.234205e-01 | 0.651 | 0 | 0 |
| Josephin domain DUBs | R-HSA-5689877 | 2.234205e-01 | 0.651 | 0 | 0 |
| Signaling by Leptin | R-HSA-2586552 | 2.234205e-01 | 0.651 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 2.238512e-01 | 0.650 | 1 | 1 |
| E2F mediated regulation of DNA replication | R-HSA-113510 | 2.272027e-01 | 0.644 | 1 | 0 |
| Rap1 signalling | R-HSA-392517 | 2.272027e-01 | 0.644 | 0 | 0 |
| RUNX3 regulates RUNX1-mediated transcription | R-HSA-8951911 | 2.393055e-01 | 0.621 | 0 | 0 |
| Regulation of cortical dendrite branching | R-HSA-8985801 | 2.393055e-01 | 0.621 | 0 | 0 |
| Enhanced cleavage of VWF variant by ADAMTS13 | R-HSA-9845619 | 2.393055e-01 | 0.621 | 0 | 0 |
| Defective VWF cleavage by ADAMTS13 variant | R-HSA-9845621 | 2.393055e-01 | 0.621 | 0 | 0 |
| Glycogen storage disease type XV (GYG1) | R-HSA-3814836 | 2.393055e-01 | 0.621 | 0 | 0 |
| Glycogen storage disease type 0 (muscle GYS1) | R-HSA-3828062 | 2.393055e-01 | 0.621 | 0 | 0 |
| Defective MMACHC causes MAHCC | R-HSA-3359474 | 2.895913e-01 | 0.538 | 0 | 0 |
| Loss of Function of KMT2D in Kabuki Syndrome | R-HSA-9944971 | 2.895913e-01 | 0.538 | 0 | 0 |
| Loss of Function of KMT2D in MLL4 Complex Formation in Kabuki Syndrome | R-HSA-9944997 | 2.895913e-01 | 0.538 | 0 | 0 |
| HCN channels | R-HSA-1296061 | 3.365558e-01 | 0.473 | 0 | 0 |
| RUNX3 regulates BCL2L11 (BIM) transcription | R-HSA-8952158 | 3.365558e-01 | 0.473 | 0 | 0 |
| PLCG1 events in ERBB2 signaling | R-HSA-1251932 | 3.365558e-01 | 0.473 | 0 | 0 |
| Drug-mediated inhibition of CDK4/CDK6 activity | R-HSA-9754119 | 3.365558e-01 | 0.473 | 0 | 0 |
| Signaling by MAP2K mutants | R-HSA-9652169 | 3.365558e-01 | 0.473 | 0 | 0 |
| GRB7 events in ERBB2 signaling | R-HSA-1306955 | 3.365558e-01 | 0.473 | 0 | 0 |
| Defective LFNG causes SCDO3 | R-HSA-5083630 | 3.365558e-01 | 0.473 | 0 | 0 |
| Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes | R-HSA-69200 | 3.365558e-01 | 0.473 | 0 | 0 |
| NOSIP mediated eNOS trafficking | R-HSA-203754 | 3.804182e-01 | 0.420 | 0 | 0 |
| Enhanced binding of GP1BA variant to VWF multimer:collagen | R-HSA-9845620 | 3.804182e-01 | 0.420 | 0 | 0 |
| Defective binding of VWF variant to GPIb:IX:V | R-HSA-9846298 | 3.804182e-01 | 0.420 | 0 | 0 |
| NR1H2 & NR1H3 regulate gene expression to control bile acid homeostasis | R-HSA-9623433 | 2.736568e-01 | 0.563 | 0 | 0 |
| Polymerase switching | R-HSA-69091 | 2.987748e-01 | 0.525 | 0 | 0 |
| Leading Strand Synthesis | R-HSA-69109 | 2.987748e-01 | 0.525 | 0 | 0 |
| GRB2 events in EGFR signaling | R-HSA-179812 | 2.987748e-01 | 0.525 | 0 | 0 |
| Defects of platelet adhesion to exposed collagen | R-HSA-9823587 | 4.213831e-01 | 0.375 | 0 | 0 |
| Nef Mediated CD8 Down-regulation | R-HSA-182218 | 4.213831e-01 | 0.375 | 0 | 0 |
| Signaling by Overexpressed Wild-Type EGFR in Cancer | R-HSA-5638302 | 4.213831e-01 | 0.375 | 0 | 0 |
| PTK6 Regulates Cell Cycle | R-HSA-8849470 | 4.213831e-01 | 0.375 | 0 | 0 |
| Inhibition of Signaling by Overexpressed EGFR | R-HSA-5638303 | 4.213831e-01 | 0.375 | 0 | 0 |
| CDC6 association with the ORC:origin complex | R-HSA-68689 | 4.213831e-01 | 0.375 | 0 | 0 |
| Loss of MECP2 binding ability to the NCoR/SMRT complex | R-HSA-9022537 | 4.213831e-01 | 0.375 | 0 | 0 |
| Signaling by RNF43 mutants | R-HSA-5340588 | 4.213831e-01 | 0.375 | 0 | 0 |
| Retrograde neurotrophin signalling | R-HSA-177504 | 3.484864e-01 | 0.458 | 0 | 0 |
| PTK6 promotes HIF1A stabilization | R-HSA-8857538 | 4.596419e-01 | 0.338 | 0 | 0 |
| Signaling by LTK in cancer | R-HSA-9842640 | 4.596419e-01 | 0.338 | 0 | 0 |
| STAT5 Activation | R-HSA-9645135 | 4.596419e-01 | 0.338 | 0 | 0 |
| Erythropoietin activates STAT5 | R-HSA-9027283 | 4.596419e-01 | 0.338 | 0 | 0 |
| Autointegration results in viral DNA circles | R-HSA-177539 | 4.596419e-01 | 0.338 | 0 | 0 |
| RNA Polymerase III Transcription Initiation From Type 3 Promoter | R-HSA-76071 | 3.001554e-01 | 0.523 | 0 | 0 |
| SHC1 events in EGFR signaling | R-HSA-180336 | 3.729116e-01 | 0.428 | 0 | 0 |
| RNA Pol II CTD phosphorylation and interaction with CE | R-HSA-77075 | 3.186634e-01 | 0.497 | 0 | 0 |
| RNA Pol II CTD phosphorylation and interaction with CE during HIV infection | R-HSA-167160 | 3.186634e-01 | 0.497 | 0 | 0 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 2.307938e-01 | 0.637 | 1 | 1 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 2.418317e-01 | 0.616 | 1 | 0 |
| Developmental Lineage of Mammary Gland Alveolar Cells | R-HSA-9927426 | 3.087334e-01 | 0.510 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 2.530219e-01 | 0.597 | 0 | 0 |
| GRB2 events in ERBB2 signaling | R-HSA-1963640 | 4.205662e-01 | 0.376 | 0 | 0 |
| Nucleosome assembly | R-HSA-774815 | 2.979868e-01 | 0.526 | 0 | 0 |
| Deposition of new CENPA-containing nucleosomes at the centromere | R-HSA-606279 | 2.979868e-01 | 0.526 | 0 | 0 |
| mRNA Splicing - Minor Pathway | R-HSA-72165 | 3.111572e-01 | 0.507 | 0 | 0 |
| Autodegradation of Cdh1 by Cdh1:APC/C | R-HSA-174084 | 3.111572e-01 | 0.507 | 0 | 0 |
| Processive synthesis on the C-strand of the telomere | R-HSA-174414 | 3.924077e-01 | 0.406 | 0 | 0 |
| Removal of the Flap Intermediate from the C-strand | R-HSA-174437 | 4.436918e-01 | 0.353 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 4.285816e-01 | 0.368 | 0 | 0 |
| Inhibition of DNA recombination at telomere | R-HSA-9670095 | 4.005537e-01 | 0.397 | 0 | 0 |
| HSF1-dependent transactivation | R-HSA-3371571 | 3.778111e-01 | 0.423 | 0 | 0 |
| Transcription-Coupled Nucleotide Excision Repair (TC-NER) | R-HSA-6781827 | 3.415024e-01 | 0.467 | 0 | 0 |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | R-HSA-9927418 | 4.458505e-01 | 0.351 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 3.869754e-01 | 0.412 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 4.436918e-01 | 0.353 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 4.436918e-01 | 0.353 | 0 | 0 |
| HIV Transcription Elongation | R-HSA-167169 | 4.005537e-01 | 0.397 | 0 | 0 |
| Degradation of beta-catenin by the destruction complex | R-HSA-195253 | 4.424094e-01 | 0.354 | 0 | 0 |
| mRNA Capping | R-HSA-72086 | 4.285816e-01 | 0.368 | 0 | 0 |
| Condensation of Prophase Chromosomes | R-HSA-2299718 | 3.111572e-01 | 0.507 | 1 | 1 |
| p75NTR recruits signalling complexes | R-HSA-209543 | 2.987748e-01 | 0.525 | 0 | 0 |
| Termination of translesion DNA synthesis | R-HSA-5656169 | 4.285816e-01 | 0.368 | 0 | 0 |
| Tat-mediated elongation of the HIV-1 transcript | R-HSA-167246 | 4.005537e-01 | 0.397 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 3.973963e-01 | 0.401 | 0 | 0 |
| TP53 Regulates Transcription of Death Receptors and Ligands | R-HSA-6803211 | 3.484864e-01 | 0.458 | 0 | 0 |
| DNA Damage Bypass | R-HSA-73893 | 3.510572e-01 | 0.455 | 0 | 0 |
| SHC1 events in ERBB2 signaling | R-HSA-1250196 | 4.463825e-01 | 0.350 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in Cytochrome C Release | R-HSA-6803204 | 3.924077e-01 | 0.406 | 0 | 0 |
| Formation of HIV-1 elongation complex containing HIV-1 Tat | R-HSA-167200 | 3.852920e-01 | 0.414 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 3.244040e-01 | 0.489 | 0 | 0 |
| p75NTR signals via NF-kB | R-HSA-193639 | 3.729116e-01 | 0.428 | 0 | 0 |
| TFAP2 (AP-2) family regulates transcription of cell cycle factors | R-HSA-8866911 | 3.365558e-01 | 0.473 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 2.987748e-01 | 0.525 | 0 | 0 |
| VLDLR internalisation and degradation | R-HSA-8866427 | 2.987748e-01 | 0.525 | 0 | 0 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | R-HSA-427389 | 4.005537e-01 | 0.397 | 0 | 0 |
| Telomere C-strand (Lagging Strand) Synthesis | R-HSA-174417 | 4.308522e-01 | 0.366 | 0 | 0 |
| NoRC negatively regulates rRNA expression | R-HSA-427413 | 4.542830e-01 | 0.343 | 0 | 0 |
| MET activates RAS signaling | R-HSA-8851805 | 2.987748e-01 | 0.525 | 0 | 0 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 4.424094e-01 | 0.354 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 3.090164e-01 | 0.510 | 0 | 0 |
| Regulation of FOXO transcriptional activity by acetylation | R-HSA-9617629 | 2.987748e-01 | 0.525 | 0 | 0 |
| JNK (c-Jun kinases) phosphorylation and activation mediated by activated human TAK1 | R-HSA-450321 | 2.633619e-01 | 0.579 | 0 | 0 |
| RNA Polymerase I Transcription Initiation | R-HSA-73762 | 2.591148e-01 | 0.587 | 0 | 0 |
| Chromatin modifications during the maternal to zygotic transition (MZT) | R-HSA-9821002 | 4.157471e-01 | 0.381 | 0 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 3.970926e-01 | 0.401 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 3.226380e-01 | 0.491 | 0 | 0 |
| G2/M Checkpoints | R-HSA-69481 | 3.804278e-01 | 0.420 | 1 | 0 |
| CRMPs in Sema3A signaling | R-HSA-399956 | 3.484864e-01 | 0.458 | 0 | 0 |
| p38MAPK events | R-HSA-171007 | 3.729116e-01 | 0.428 | 0 | 0 |
| WNT5A-dependent internalization of FZD4 | R-HSA-5099900 | 3.969570e-01 | 0.401 | 0 | 0 |
| Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters | R-HSA-164938 | 4.436918e-01 | 0.353 | 0 | 0 |
| Regulation of gene expression by Hypoxia-inducible Factor | R-HSA-1234158 | 2.736568e-01 | 0.563 | 0 | 0 |
| Telomere Maintenance | R-HSA-157579 | 4.585303e-01 | 0.339 | 0 | 0 |
| Leishmania phagocytosis | R-HSA-9664417 | 3.889116e-01 | 0.410 | 0 | 0 |
| Parasite infection | R-HSA-9664407 | 3.889116e-01 | 0.410 | 0 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 3.889116e-01 | 0.410 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 4.099167e-01 | 0.387 | 1 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 3.693809e-01 | 0.433 | 0 | 0 |
| Negative regulation of TCF-dependent signaling by DVL-interacting proteins | R-HSA-5368598 | 2.895913e-01 | 0.538 | 0 | 0 |
| Loss of MECP2 binding ability to 5mC-DNA | R-HSA-9022538 | 2.895913e-01 | 0.538 | 0 | 0 |
| SARS-CoV-2 targets PDZ proteins in cell-cell junction | R-HSA-9705677 | 3.365558e-01 | 0.473 | 0 | 0 |
| Reelin signalling pathway | R-HSA-8866376 | 3.804182e-01 | 0.420 | 0 | 0 |
| NFE2L2 regulates pentose phosphate pathway genes | R-HSA-9818028 | 2.736568e-01 | 0.563 | 0 | 0 |
| Mitotic Telophase/Cytokinesis | R-HSA-68884 | 2.736568e-01 | 0.563 | 0 | 0 |
| Signalling to RAS | R-HSA-167044 | 2.633619e-01 | 0.579 | 0 | 0 |
| Regulation of CDH1 mRNA translation by microRNAs | R-HSA-9764562 | 3.484864e-01 | 0.458 | 0 | 0 |
| G2/M DNA replication checkpoint | R-HSA-69478 | 4.596419e-01 | 0.338 | 1 | 1 |
| Regulation of FZD by ubiquitination | R-HSA-4641263 | 4.436918e-01 | 0.353 | 0 | 0 |
| G2/M DNA damage checkpoint | R-HSA-69473 | 3.306175e-01 | 0.481 | 1 | 0 |
| Transcriptional regulation of brown and beige adipocyte differentiation | R-HSA-9843743 | 4.005537e-01 | 0.397 | 0 | 0 |
| Transcriptional regulation of brown and beige adipocyte differentiation by EBF2 | R-HSA-9844594 | 4.005537e-01 | 0.397 | 0 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 3.886300e-01 | 0.410 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 2.411650e-01 | 0.618 | 0 | 0 |
| Activation of BH3-only proteins | R-HSA-114452 | 2.340784e-01 | 0.631 | 0 | 0 |
| Neurexins and neuroligins | R-HSA-6794361 | 2.307938e-01 | 0.637 | 0 | 0 |
| Resolution of AP sites via the multiple-nucleotide patch replacement pathway | R-HSA-110373 | 3.740942e-01 | 0.427 | 0 | 0 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | R-HSA-166058 | 4.249624e-01 | 0.372 | 0 | 0 |
| Aggrephagy | R-HSA-9646399 | 4.005537e-01 | 0.397 | 0 | 0 |
| Toll Like Receptor TLR6:TLR2 Cascade | R-HSA-168188 | 4.249624e-01 | 0.372 | 0 | 0 |
| Toll Like Receptor TLR1:TLR2 Cascade | R-HSA-168179 | 4.520411e-01 | 0.345 | 0 | 0 |
| Signaling by FGFR1 in disease | R-HSA-5655302 | 4.308522e-01 | 0.366 | 0 | 0 |
| Transcriptional Regulation by E2F6 | R-HSA-8953750 | 3.852920e-01 | 0.414 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 2.403350e-01 | 0.619 | 1 | 0 |
| Toll Like Receptor 2 (TLR2) Cascade | R-HSA-181438 | 4.520411e-01 | 0.345 | 0 | 0 |
| Early Phase of HIV Life Cycle | R-HSA-162594 | 2.633619e-01 | 0.579 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 4.402282e-01 | 0.356 | 0 | 0 |
| Acetylcholine regulates insulin secretion | R-HSA-399997 | 4.205662e-01 | 0.376 | 0 | 0 |
| Energy dependent regulation of mTOR by LKB1-AMPK | R-HSA-380972 | 4.463825e-01 | 0.350 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 4.486069e-01 | 0.348 | 0 | 0 |
| Negative regulation of MET activity | R-HSA-6807004 | 2.451763e-01 | 0.611 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 2.443911e-01 | 0.612 | 1 | 0 |
| Loss of function of MECP2 in Rett syndrome | R-HSA-9005891 | 2.987748e-01 | 0.525 | 0 | 0 |
| Pervasive developmental disorders | R-HSA-9005895 | 2.987748e-01 | 0.525 | 0 | 0 |
| Disorders of Nervous System Development | R-HSA-9697154 | 2.987748e-01 | 0.525 | 0 | 0 |
| Regulation of CDH19 Expression and Function | R-HSA-9764302 | 4.213831e-01 | 0.375 | 0 | 0 |
| Dopamine Neurotransmitter Release Cycle | R-HSA-212676 | 3.001554e-01 | 0.523 | 0 | 0 |
| TNF signaling | R-HSA-75893 | 2.758078e-01 | 0.559 | 0 | 0 |
| MyD88 dependent cascade initiated on endosome | R-HSA-975155 | 4.456520e-01 | 0.351 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 2.483312e-01 | 0.605 | 0 | 0 |
| Regulation of KIT signaling | R-HSA-1433559 | 3.484864e-01 | 0.458 | 0 | 0 |
| E3 ubiquitin ligases ubiquitinate target proteins | R-HSA-8866654 | 3.911856e-01 | 0.408 | 0 | 0 |
| MyD88 cascade initiated on plasma membrane | R-HSA-975871 | 3.312768e-01 | 0.480 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 3.106264e-01 | 0.508 | 0 | 0 |
| Toll Like Receptor 10 (TLR10) Cascade | R-HSA-168142 | 3.312768e-01 | 0.480 | 0 | 0 |
| Toll Like Receptor 5 (TLR5) Cascade | R-HSA-168176 | 3.312768e-01 | 0.480 | 0 | 0 |
| Formation of the dystrophin-glycoprotein complex (DGC) | R-HSA-9913351 | 2.486912e-01 | 0.604 | 0 | 0 |
| Homology Directed Repair | R-HSA-5693538 | 4.159184e-01 | 0.381 | 0 | 0 |
| Reproduction | R-HSA-1474165 | 4.147428e-01 | 0.382 | 0 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 4.005537e-01 | 0.397 | 0 | 0 |
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | R-HSA-975138 | 4.361051e-01 | 0.360 | 0 | 0 |
| Toll Like Receptor 9 (TLR9) Cascade | R-HSA-168138 | 3.797785e-01 | 0.420 | 0 | 0 |
| Diseases of Mismatch Repair (MMR) | R-HSA-5423599 | 2.895913e-01 | 0.538 | 0 | 0 |
| Sensory perception of sour taste | R-HSA-9729555 | 3.365558e-01 | 0.473 | 0 | 0 |
| Signalling to p38 via RIT and RIN | R-HSA-187706 | 4.213831e-01 | 0.375 | 0 | 0 |
| Integration of viral DNA into host genomic DNA | R-HSA-175567 | 4.596419e-01 | 0.338 | 0 | 0 |
| Base Excision Repair | R-HSA-73884 | 3.667842e-01 | 0.436 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 3.584594e-01 | 0.446 | 0 | 0 |
| Signaling by NTRK3 (TRKC) | R-HSA-9034015 | 2.817054e-01 | 0.550 | 0 | 0 |
| Smooth Muscle Contraction | R-HSA-445355 | 4.045381e-01 | 0.393 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 2.370237e-01 | 0.625 | 0 | 0 |
| Formation of definitive endoderm | R-HSA-9823730 | 2.451763e-01 | 0.611 | 0 | 0 |
| FLT3 Signaling | R-HSA-9607240 | 2.339174e-01 | 0.631 | 0 | 0 |
| PECAM1 interactions | R-HSA-210990 | 2.484987e-01 | 0.605 | 0 | 0 |
| TBC/RABGAPs | R-HSA-8854214 | 2.719473e-01 | 0.566 | 0 | 0 |
| Ovarian tumor domain proteases | R-HSA-5689896 | 3.546488e-01 | 0.450 | 1 | 1 |
| Spry regulation of FGF signaling | R-HSA-1295596 | 3.729116e-01 | 0.428 | 0 | 0 |
| Regulation of beta-cell development | R-HSA-186712 | 3.108054e-01 | 0.508 | 0 | 0 |
| Regulation of RUNX1 Expression and Activity | R-HSA-8934593 | 3.740942e-01 | 0.427 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 3.464774e-01 | 0.460 | 0 | 0 |
| tRNA-derived small RNA (tsRNA or tRNA-related fragment, tRF) biogenesis | R-HSA-9708296 | 2.393055e-01 | 0.621 | 0 | 0 |
| The NLRP1 inflammasome | R-HSA-844455 | 2.895913e-01 | 0.538 | 0 | 0 |
| Anchoring fibril formation | R-HSA-2214320 | 2.736568e-01 | 0.563 | 0 | 0 |
| HDR through MMEJ (alt-NHEJ) | R-HSA-5685939 | 3.237481e-01 | 0.490 | 0 | 0 |
| PI5P Regulates TP53 Acetylation | R-HSA-6811555 | 3.237481e-01 | 0.490 | 0 | 0 |
| NADPH regeneration | R-HSA-389542 | 4.596419e-01 | 0.338 | 0 | 0 |
| Fibronectin matrix formation | R-HSA-1566977 | 4.205662e-01 | 0.376 | 0 | 0 |
| Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian Skin | R-HSA-9725554 | 3.852920e-01 | 0.414 | 0 | 0 |
| Orc1 removal from chromatin | R-HSA-68949 | 3.911856e-01 | 0.408 | 0 | 0 |
| Non-integrin membrane-ECM interactions | R-HSA-3000171 | 3.415024e-01 | 0.467 | 0 | 0 |
| MECP2 regulates neuronal receptors and channels | R-HSA-9022699 | 3.740942e-01 | 0.427 | 0 | 0 |
| Myogenesis | R-HSA-525793 | 3.740942e-01 | 0.427 | 0 | 0 |
| TRIF (TICAM1)-mediated TLR4 signaling | R-HSA-937061 | 4.551778e-01 | 0.342 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 3.360654e-01 | 0.474 | 0 | 0 |
| Intrinsic Pathway for Apoptosis | R-HSA-109606 | 4.443207e-01 | 0.352 | 0 | 0 |
| MyD88-independent TLR4 cascade | R-HSA-166166 | 4.551778e-01 | 0.342 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 2.529434e-01 | 0.597 | 0 | 0 |
| Toll Like Receptor 3 (TLR3) Cascade | R-HSA-168164 | 4.073911e-01 | 0.390 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in apoptosis | R-HSA-9824594 | 2.633619e-01 | 0.579 | 0 | 0 |
| Cyclin A/B1/B2 associated events during G2/M transition | R-HSA-69273 | 2.784523e-01 | 0.555 | 1 | 1 |
| PTEN Regulation | R-HSA-6807070 | 2.746913e-01 | 0.561 | 0 | 0 |
| CREB3 factors activate genes | R-HSA-8874211 | 4.596419e-01 | 0.338 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 4.585303e-01 | 0.339 | 0 | 0 |
| FOXO-mediated transcription | R-HSA-9614085 | 3.406864e-01 | 0.468 | 0 | 0 |
| Regulation of Expression and Function of Type II Classical Cadherins | R-HSA-9764260 | 2.784523e-01 | 0.555 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 3.505785e-01 | 0.455 | 0 | 0 |
| Collagen chain trimerization | R-HSA-8948216 | 3.546488e-01 | 0.450 | 0 | 0 |
| Neurofascin interactions | R-HSA-447043 | 4.596419e-01 | 0.338 | 0 | 0 |
| SARS-CoV-1 targets host intracellular signalling and regulatory pathways | R-HSA-9735871 | 3.729116e-01 | 0.428 | 0 | 0 |
| Regulation of CDH11 Expression and Function | R-HSA-9759475 | 4.285816e-01 | 0.368 | 0 | 0 |
| tRNA processing | R-HSA-72306 | 3.163198e-01 | 0.500 | 0 | 0 |
| OAS antiviral response | R-HSA-8983711 | 2.987748e-01 | 0.525 | 0 | 0 |
| MAP3K8 (TPL2)-dependent MAPK1/3 activation | R-HSA-5684264 | 3.484864e-01 | 0.458 | 0 | 0 |
| Defective Intrinsic Pathway for Apoptosis | R-HSA-9734009 | 3.924077e-01 | 0.406 | 0 | 0 |
| Miscellaneous transport and binding events | R-HSA-5223345 | 2.935420e-01 | 0.532 | 0 | 0 |
| Glucose metabolism | R-HSA-70326 | 2.883945e-01 | 0.540 | 0 | 0 |
| Interleukin-7 signaling | R-HSA-1266695 | 3.556740e-01 | 0.449 | 0 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 4.607243e-01 | 0.337 | 0 | 0 |
| Trafficking of AMPA receptors | R-HSA-399719 | 4.639574e-01 | 0.334 | 0 | 0 |
| Evasion by RSV of host interferon responses | R-HSA-9833109 | 4.639574e-01 | 0.334 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 4.644088e-01 | 0.333 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 4.662945e-01 | 0.331 | 0 | 0 |
| Regulation of TP53 Activity through Methylation | R-HSA-6804760 | 4.662945e-01 | 0.331 | 0 | 0 |
| Trafficking of GluR2-containing AMPA receptors | R-HSA-416993 | 4.662945e-01 | 0.331 | 0 | 0 |
| Tie2 Signaling | R-HSA-210993 | 4.662945e-01 | 0.331 | 0 | 0 |
| FOXO-mediated transcription of cell death genes | R-HSA-9614657 | 4.662945e-01 | 0.331 | 0 | 0 |
| Nephron development | R-HSA-9831926 | 4.662945e-01 | 0.331 | 0 | 0 |
| Gap junction trafficking | R-HSA-190828 | 4.754573e-01 | 0.323 | 0 | 0 |
| RMTs methylate histone arginines | R-HSA-3214858 | 4.754573e-01 | 0.323 | 0 | 0 |
| HCMV Infection | R-HSA-9609646 | 4.811381e-01 | 0.318 | 0 | 0 |
| Signaling by WNT in cancer | R-HSA-4791275 | 4.812832e-01 | 0.318 | 0 | 0 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | R-HSA-5693565 | 4.834164e-01 | 0.316 | 0 | 0 |
| Toll Like Receptor 7/8 (TLR7/8) Cascade | R-HSA-168181 | 4.835780e-01 | 0.316 | 0 | 0 |
| Crosslinking of collagen fibrils | R-HSA-2243919 | 4.883426e-01 | 0.311 | 0 | 0 |
| Signaling by FGFR2 IIIa TM | R-HSA-8851708 | 4.883426e-01 | 0.311 | 0 | 0 |
| Gastrin-CREB signalling pathway via PKC and MAPK | R-HSA-881907 | 4.883426e-01 | 0.311 | 0 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 4.883426e-01 | 0.311 | 0 | 0 |
| Signaling by NOTCH4 | R-HSA-9013694 | 4.895099e-01 | 0.310 | 0 | 0 |
| Signaling by FGFR in disease | R-HSA-1226099 | 4.895099e-01 | 0.310 | 0 | 0 |
| Selective autophagy | R-HSA-9663891 | 4.944662e-01 | 0.306 | 0 | 0 |
| RUNX3 Regulates Immune Response and Cell Migration | R-HSA-8949275 | 4.953731e-01 | 0.305 | 0 | 0 |
| IFNG signaling activates MAPKs | R-HSA-9732724 | 4.953731e-01 | 0.305 | 0 | 0 |
| NR1H2 & NR1H3 regulate gene expression linked to triglyceride lipolysis in adipose | R-HSA-9031528 | 4.953731e-01 | 0.305 | 0 | 0 |
| Pre-NOTCH Processing in the Endoplasmic Reticulum | R-HSA-1912399 | 4.953731e-01 | 0.305 | 0 | 0 |
| Disinhibition of SNARE formation | R-HSA-114516 | 4.953731e-01 | 0.305 | 0 | 0 |
| Recycling of eIF2:GDP | R-HSA-72731 | 4.953731e-01 | 0.305 | 0 | 0 |
| NR1H2 & NR1H3 regulate gene expression to limit cholesterol uptake | R-HSA-9031525 | 4.953731e-01 | 0.305 | 0 | 0 |
| PTK6 Expression | R-HSA-8849473 | 4.953731e-01 | 0.305 | 0 | 0 |
| Nef Mediated CD4 Down-regulation | R-HSA-167590 | 4.953731e-01 | 0.305 | 0 | 0 |
| VLDL clearance | R-HSA-8964046 | 4.953731e-01 | 0.305 | 0 | 0 |
| Regulation of PTEN localization | R-HSA-8948747 | 4.953731e-01 | 0.305 | 0 | 0 |
| Netrin mediated repulsion signals | R-HSA-418886 | 4.953731e-01 | 0.305 | 0 | 0 |
| FGFR1 mutant receptor activation | R-HSA-1839124 | 4.983389e-01 | 0.302 | 0 | 0 |
| Glutamate binding, activation of AMPA receptors and synaptic plasticity | R-HSA-399721 | 4.983389e-01 | 0.302 | 0 | 0 |
| Regulation of MECP2 expression and activity | R-HSA-9022692 | 4.983389e-01 | 0.302 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 5.036846e-01 | 0.298 | 0 | 0 |
| IRS-related events triggered by IGF1R | R-HSA-2428928 | 5.089429e-01 | 0.293 | 0 | 0 |
| VxPx cargo-targeting to cilium | R-HSA-5620916 | 5.098104e-01 | 0.293 | 0 | 0 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | R-HSA-9609523 | 5.098104e-01 | 0.293 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 5.098104e-01 | 0.293 | 0 | 0 |
| Nephrin family interactions | R-HSA-373753 | 5.098104e-01 | 0.293 | 0 | 0 |
| RNA Polymerase I Promoter Clearance | R-HSA-73854 | 5.125806e-01 | 0.290 | 0 | 0 |
| Striated Muscle Contraction | R-HSA-390522 | 5.151061e-01 | 0.288 | 0 | 0 |
| Association of TriC/CCT with target proteins during biosynthesis | R-HSA-390471 | 5.151061e-01 | 0.288 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 5.168549e-01 | 0.287 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 5.191643e-01 | 0.285 | 0 | 0 |
| Synthesis of PIPs at the plasma membrane | R-HSA-1660499 | 5.215141e-01 | 0.283 | 0 | 0 |
| NR1H2 and NR1H3-mediated signaling | R-HSA-9024446 | 5.239681e-01 | 0.281 | 0 | 0 |
| Transcriptional Regulation by MECP2 | R-HSA-8986944 | 5.261630e-01 | 0.279 | 0 | 0 |
| EGFR interacts with phospholipase C-gamma | R-HSA-212718 | 5.287436e-01 | 0.277 | 0 | 0 |
| MET receptor recycling | R-HSA-8875656 | 5.287436e-01 | 0.277 | 0 | 0 |
| Myoclonic epilepsy of Lafora | R-HSA-3785653 | 5.287436e-01 | 0.277 | 0 | 0 |
| Nef mediated downregulation of MHC class I complex cell surface expression | R-HSA-164940 | 5.287436e-01 | 0.277 | 0 | 0 |
| Adrenoceptors | R-HSA-390696 | 5.287436e-01 | 0.277 | 0 | 0 |
| Axonal growth inhibition (RHOA activation) | R-HSA-193634 | 5.287436e-01 | 0.277 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of myeloid cells | R-HSA-8939246 | 5.287436e-01 | 0.277 | 0 | 0 |
| Sodium/Proton exchangers | R-HSA-425986 | 5.287436e-01 | 0.277 | 0 | 0 |
| Downregulation of ERBB4 signaling | R-HSA-1253288 | 5.287436e-01 | 0.277 | 0 | 0 |
| Activated NTRK2 signals through FYN | R-HSA-9032500 | 5.287436e-01 | 0.277 | 0 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 5.306783e-01 | 0.275 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 5.306783e-01 | 0.275 | 0 | 0 |
| TNFR1-induced proapoptotic signaling | R-HSA-5357786 | 5.306783e-01 | 0.275 | 0 | 0 |
| BMAL1:CLOCK,NPAS2 activates circadian expression | R-HSA-1368108 | 5.315685e-01 | 0.274 | 0 | 0 |
| Dual Incision in GG-NER | R-HSA-5696400 | 5.315685e-01 | 0.274 | 0 | 0 |
| Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | R-HSA-9843970 | 5.315685e-01 | 0.274 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | R-HSA-110328 | 5.315685e-01 | 0.274 | 0 | 0 |
| Mitophagy | R-HSA-5205647 | 5.315685e-01 | 0.274 | 0 | 0 |
| Nonhomologous End-Joining (NHEJ) | R-HSA-5693571 | 5.326934e-01 | 0.274 | 0 | 0 |
| RNA Polymerase I Transcription | R-HSA-73864 | 5.352476e-01 | 0.271 | 0 | 0 |
| Rab regulation of trafficking | R-HSA-9007101 | 5.391567e-01 | 0.268 | 0 | 0 |
| Mitochondrial biogenesis | R-HSA-1592230 | 5.391567e-01 | 0.268 | 0 | 0 |
| IGF1R signaling cascade | R-HSA-2428924 | 5.462277e-01 | 0.263 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 5.482111e-01 | 0.261 | 0 | 0 |
| RNA Polymerase III Transcription Initiation From Type 2 Promoter | R-HSA-76066 | 5.509319e-01 | 0.259 | 0 | 0 |
| activated TAK1 mediates p38 MAPK activation | R-HSA-450302 | 5.509319e-01 | 0.259 | 0 | 0 |
| Listeria monocytogenes entry into host cells | R-HSA-8876384 | 5.509319e-01 | 0.259 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 5.515770e-01 | 0.258 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 5.560818e-01 | 0.255 | 0 | 0 |
| Negative epigenetic regulation of rRNA expression | R-HSA-5250941 | 5.574561e-01 | 0.254 | 0 | 0 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | R-HSA-2404192 | 5.583539e-01 | 0.253 | 0 | 0 |
| Activation of the AP-1 family of transcription factors | R-HSA-450341 | 5.599091e-01 | 0.252 | 0 | 0 |
| p75NTR regulates axonogenesis | R-HSA-193697 | 5.599091e-01 | 0.252 | 0 | 0 |
| Regulation of signaling by NODAL | R-HSA-1433617 | 5.599091e-01 | 0.252 | 0 | 0 |
| WNT mediated activation of DVL | R-HSA-201688 | 5.599091e-01 | 0.252 | 0 | 0 |
| AKT phosphorylates targets in the nucleus | R-HSA-198693 | 5.599091e-01 | 0.252 | 0 | 0 |
| Cellular response to mitochondrial stress | R-HSA-9840373 | 5.599091e-01 | 0.252 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 5.659726e-01 | 0.247 | 0 | 0 |
| Collagen formation | R-HSA-1474290 | 5.671810e-01 | 0.246 | 0 | 0 |
| Processing of DNA double-strand break ends | R-HSA-5693607 | 5.683730e-01 | 0.245 | 0 | 0 |
| FGFR2 alternative splicing | R-HSA-6803529 | 5.705611e-01 | 0.244 | 0 | 0 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | R-HSA-9670439 | 5.705611e-01 | 0.244 | 0 | 0 |
| RNA Polymerase III Transcription Initiation From Type 1 Promoter | R-HSA-76061 | 5.705611e-01 | 0.244 | 0 | 0 |
| Signaling by KIT in disease | R-HSA-9669938 | 5.705611e-01 | 0.244 | 0 | 0 |
| Downregulation of TGF-beta receptor signaling | R-HSA-2173788 | 5.705611e-01 | 0.244 | 0 | 0 |
| LDL clearance | R-HSA-8964038 | 5.705611e-01 | 0.244 | 0 | 0 |
| TRAF6 mediated IRF7 activation | R-HSA-933541 | 5.789938e-01 | 0.237 | 0 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 5.809574e-01 | 0.236 | 0 | 0 |
| Toll Like Receptor 4 (TLR4) Cascade | R-HSA-166016 | 5.819519e-01 | 0.235 | 0 | 0 |
| DNA Double Strand Break Response | R-HSA-5693606 | 5.821093e-01 | 0.235 | 0 | 0 |
| Uptake and actions of bacterial toxins | R-HSA-5339562 | 5.866555e-01 | 0.232 | 0 | 0 |
| MAPK3 (ERK1) activation | R-HSA-110056 | 5.890154e-01 | 0.230 | 1 | 1 |
| Erythropoietin activates Phospholipase C gamma (PLCG) | R-HSA-9027277 | 5.890154e-01 | 0.230 | 0 | 0 |
| DNA replication initiation | R-HSA-68952 | 5.890154e-01 | 0.230 | 0 | 0 |
| Folding of actin by CCT/TriC | R-HSA-390450 | 5.890154e-01 | 0.230 | 0 | 0 |
| Binding and entry of HIV virion | R-HSA-173107 | 5.890154e-01 | 0.230 | 0 | 0 |
| WNT5A-dependent internalization of FZD2, FZD5 and ROR2 | R-HSA-5140745 | 5.890154e-01 | 0.230 | 0 | 0 |
| Formation of intermediate mesoderm | R-HSA-9761174 | 5.890154e-01 | 0.230 | 0 | 0 |
| 2-LTR circle formation | R-HSA-164843 | 5.890154e-01 | 0.230 | 0 | 0 |
| MECP2 regulates transcription of neuronal ligands | R-HSA-9022702 | 5.890154e-01 | 0.230 | 0 | 0 |
| Regulation of CDH11 function | R-HSA-9762292 | 5.890154e-01 | 0.230 | 0 | 0 |
| Response of EIF2AK1 (HRI) to heme deficiency | R-HSA-9648895 | 5.895599e-01 | 0.229 | 0 | 0 |
| The role of Nef in HIV-1 replication and disease pathogenesis | R-HSA-164952 | 5.895599e-01 | 0.229 | 0 | 0 |
| Syndecan interactions | R-HSA-3000170 | 5.895599e-01 | 0.229 | 0 | 0 |
| Growth hormone receptor signaling | R-HSA-982772 | 5.895599e-01 | 0.229 | 0 | 0 |
| Gastrulation | R-HSA-9758941 | 5.898261e-01 | 0.229 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 5.956099e-01 | 0.225 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 5.968352e-01 | 0.224 | 0 | 0 |
| Meiotic synapsis | R-HSA-1221632 | 5.995660e-01 | 0.222 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 6.003097e-01 | 0.222 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 6.071764e-01 | 0.217 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 6.079259e-01 | 0.216 | 0 | 0 |
| Replacement of protamines by nucleosomes in the male pronucleus | R-HSA-9821993 | 6.079259e-01 | 0.216 | 0 | 0 |
| Signaling by FLT3 ITD and TKD mutants | R-HSA-9703648 | 6.079259e-01 | 0.216 | 0 | 0 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | R-HSA-8862803 | 6.079259e-01 | 0.216 | 0 | 0 |
| Neurodegenerative Diseases | R-HSA-8863678 | 6.079259e-01 | 0.216 | 0 | 0 |
| Plasma lipoprotein clearance | R-HSA-8964043 | 6.088758e-01 | 0.215 | 0 | 0 |
| MAPK6/MAPK4 signaling | R-HSA-5687128 | 6.106683e-01 | 0.214 | 1 | 1 |
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | R-HSA-933543 | 6.161983e-01 | 0.210 | 0 | 0 |
| Signaling by APC mutants | R-HSA-4839744 | 6.161983e-01 | 0.210 | 0 | 0 |
| AXIN missense mutants destabilize the destruction complex | R-HSA-5467340 | 6.161983e-01 | 0.210 | 0 | 0 |
| Truncations of AMER1 destabilize the destruction complex | R-HSA-5467348 | 6.161983e-01 | 0.210 | 0 | 0 |
| APC truncation mutants have impaired AXIN binding | R-HSA-5467337 | 6.161983e-01 | 0.210 | 0 | 0 |
| LGI-ADAM interactions | R-HSA-5682910 | 6.161983e-01 | 0.210 | 0 | 0 |
| Activated NTRK3 signals through RAS | R-HSA-9034864 | 6.161983e-01 | 0.210 | 0 | 0 |
| InlA-mediated entry of Listeria monocytogenes into host cells | R-HSA-8876493 | 6.161983e-01 | 0.210 | 0 | 0 |
| Synthesis of PI | R-HSA-1483226 | 6.161983e-01 | 0.210 | 0 | 0 |
| Inorganic anion exchange by SLC26 transporters | R-HSA-427601 | 6.161983e-01 | 0.210 | 0 | 0 |
| Suppression of apoptosis | R-HSA-9635465 | 6.161983e-01 | 0.210 | 0 | 0 |
| Interleukin-2 signaling | R-HSA-9020558 | 6.161983e-01 | 0.210 | 0 | 0 |
| Regulation of endogenous retroelements by KRAB-ZFP proteins | R-HSA-9843940 | 6.164094e-01 | 0.210 | 0 | 0 |
| Regulation of RUNX3 expression and activity | R-HSA-8941858 | 6.232750e-01 | 0.205 | 0 | 0 |
| Attenuation phase | R-HSA-3371568 | 6.232750e-01 | 0.205 | 0 | 0 |
| Nuclear signaling by ERBB4 | R-HSA-1251985 | 6.232750e-01 | 0.205 | 0 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 6.246453e-01 | 0.204 | 0 | 0 |
| Long-term potentiation | R-HSA-9620244 | 6.256595e-01 | 0.204 | 0 | 0 |
| Acyl chain remodelling of PS | R-HSA-1482801 | 6.256595e-01 | 0.204 | 0 | 0 |
| Polymerase switching on the C-strand of the telomere | R-HSA-174411 | 6.256595e-01 | 0.204 | 0 | 0 |
| Laminin interactions | R-HSA-3000157 | 6.256595e-01 | 0.204 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 6.256595e-01 | 0.204 | 0 | 0 |
| Transcriptional and post-translational regulation of MITF-M expression and activity | R-HSA-9856649 | 6.274671e-01 | 0.202 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 6.287182e-01 | 0.202 | 0 | 0 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | R-HSA-5693567 | 6.299268e-01 | 0.201 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 6.318164e-01 | 0.199 | 1 | 0 |
| Platelet degranulation | R-HSA-114608 | 6.343667e-01 | 0.198 | 0 | 0 |
| Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 | R-HSA-5625886 | 6.373071e-01 | 0.196 | 0 | 0 |
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | R-HSA-110313 | 6.373071e-01 | 0.196 | 0 | 0 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | R-HSA-450531 | 6.383302e-01 | 0.195 | 0 | 0 |
| Signaling by GSK3beta mutants | R-HSA-5339716 | 6.415848e-01 | 0.193 | 0 | 0 |
| Integration of provirus | R-HSA-162592 | 6.415848e-01 | 0.193 | 0 | 0 |
| Negative regulation of TCF-dependent signaling by WNT ligand antagonists | R-HSA-3772470 | 6.415848e-01 | 0.193 | 0 | 0 |
| NF-kB is activated and signals survival | R-HSA-209560 | 6.415848e-01 | 0.193 | 0 | 0 |
| Activated NTRK2 signals through RAS | R-HSA-9026519 | 6.415848e-01 | 0.193 | 0 | 0 |
| ERKs are inactivated | R-HSA-202670 | 6.415848e-01 | 0.193 | 0 | 0 |
| Signaling by AXIN mutants | R-HSA-4839735 | 6.415848e-01 | 0.193 | 0 | 0 |
| Signaling by AMER1 mutants | R-HSA-4839748 | 6.415848e-01 | 0.193 | 0 | 0 |
| APOBEC3G mediated resistance to HIV-1 infection | R-HSA-180689 | 6.415848e-01 | 0.193 | 0 | 0 |
| POLB-Dependent Long Patch Base Excision Repair | R-HSA-110362 | 6.415848e-01 | 0.193 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 6.415848e-01 | 0.193 | 1 | 1 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 6.427642e-01 | 0.192 | 0 | 0 |
| MET activates PTK2 signaling | R-HSA-8874081 | 6.427642e-01 | 0.192 | 0 | 0 |
| Activated NOTCH1 Transmits Signal to the Nucleus | R-HSA-2122948 | 6.427642e-01 | 0.192 | 0 | 0 |
| Synthesis of PIPs at the Golgi membrane | R-HSA-1660514 | 6.427642e-01 | 0.192 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 6.429576e-01 | 0.192 | 0 | 0 |
| IRS-mediated signalling | R-HSA-112399 | 6.487047e-01 | 0.188 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 6.487047e-01 | 0.188 | 0 | 0 |
| Ca2+ pathway | R-HSA-4086398 | 6.489952e-01 | 0.188 | 0 | 0 |
| FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | R-HSA-9615017 | 6.509693e-01 | 0.186 | 0 | 0 |
| PI Metabolism | R-HSA-1483255 | 6.528313e-01 | 0.185 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 6.540438e-01 | 0.184 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 6.592455e-01 | 0.181 | 0 | 0 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | R-HSA-4641262 | 6.592455e-01 | 0.181 | 0 | 0 |
| RNA Polymerase I Transcription Termination | R-HSA-73863 | 6.592455e-01 | 0.181 | 0 | 0 |
| TNFR1-induced NF-kappa-B signaling pathway | R-HSA-5357956 | 6.592455e-01 | 0.181 | 0 | 0 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 6.592455e-01 | 0.181 | 0 | 0 |
| Signaling by ERBB4 | R-HSA-1236394 | 6.594593e-01 | 0.181 | 0 | 0 |
| Dual incision in TC-NER | R-HSA-6782135 | 6.603432e-01 | 0.180 | 0 | 0 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | R-HSA-72662 | 6.603432e-01 | 0.180 | 0 | 0 |
| NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux | R-HSA-9029569 | 6.603432e-01 | 0.180 | 0 | 0 |
| Cleavage of the damaged pyrimidine | R-HSA-110329 | 6.642599e-01 | 0.178 | 0 | 0 |
| Depyrimidination | R-HSA-73928 | 6.642599e-01 | 0.178 | 0 | 0 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | R-HSA-9027276 | 6.652936e-01 | 0.177 | 0 | 0 |
| IRAK1 recruits IKK complex upon TLR7/8 or 9 stimulation | R-HSA-975144 | 6.652936e-01 | 0.177 | 0 | 0 |
| IRAK1 recruits IKK complex | R-HSA-937039 | 6.652936e-01 | 0.177 | 0 | 0 |
| Signaling by CTNNB1 phospho-site mutants | R-HSA-4839743 | 6.652936e-01 | 0.177 | 0 | 0 |
| Scavenging by Class F Receptors | R-HSA-3000484 | 6.652936e-01 | 0.177 | 0 | 0 |
| CTNNB1 S33 mutants aren't phosphorylated | R-HSA-5358747 | 6.652936e-01 | 0.177 | 0 | 0 |
| CTNNB1 T41 mutants aren't phosphorylated | R-HSA-5358752 | 6.652936e-01 | 0.177 | 0 | 0 |
| CTNNB1 S45 mutants aren't phosphorylated | R-HSA-5358751 | 6.652936e-01 | 0.177 | 0 | 0 |
| CTNNB1 S37 mutants aren't phosphorylated | R-HSA-5358749 | 6.652936e-01 | 0.177 | 0 | 0 |
| SHC-related events triggered by IGF1R | R-HSA-2428933 | 6.652936e-01 | 0.177 | 0 | 0 |
| Downregulation of ERBB2:ERBB3 signaling | R-HSA-1358803 | 6.652936e-01 | 0.177 | 0 | 0 |
| Activated NTRK2 signals through FRS2 and FRS3 | R-HSA-9028731 | 6.652936e-01 | 0.177 | 0 | 0 |
| Constitutive Signaling by Overexpressed ERBB2 | R-HSA-9634285 | 6.652936e-01 | 0.177 | 0 | 0 |
| Advanced glycosylation endproduct receptor signaling | R-HSA-879415 | 6.652936e-01 | 0.177 | 0 | 0 |
| Regulation of IFNG signaling | R-HSA-877312 | 6.652936e-01 | 0.177 | 0 | 0 |
| TP53 Regulates Transcription of Cell Death Genes | R-HSA-5633008 | 6.697200e-01 | 0.174 | 0 | 0 |
| Protein ubiquitination | R-HSA-8852135 | 6.697200e-01 | 0.174 | 0 | 0 |
| Cilium Assembly | R-HSA-5617833 | 6.708698e-01 | 0.173 | 1 | 0 |
| Extension of Telomeres | R-HSA-180786 | 6.717176e-01 | 0.173 | 0 | 0 |
| Negative regulation of FGFR3 signaling | R-HSA-5654732 | 6.751110e-01 | 0.171 | 0 | 0 |
| Signaling by FGFR4 | R-HSA-5654743 | 6.771784e-01 | 0.169 | 0 | 0 |
| RSV-host interactions | R-HSA-9833110 | 6.790172e-01 | 0.168 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 6.815065e-01 | 0.167 | 0 | 0 |
| Kinesins | R-HSA-983189 | 6.828265e-01 | 0.166 | 0 | 0 |
| Platelet Adhesion to exposed collagen | R-HSA-75892 | 6.874354e-01 | 0.163 | 0 | 0 |
| Formation of axial mesoderm | R-HSA-9796292 | 6.874354e-01 | 0.163 | 0 | 0 |
| Acyl chain remodeling of DAG and TAG | R-HSA-1482883 | 6.874354e-01 | 0.163 | 0 | 0 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | R-HSA-75035 | 6.874354e-01 | 0.163 | 1 | 1 |
| Golgi Cisternae Pericentriolar Stack Reorganization | R-HSA-162658 | 6.874354e-01 | 0.163 | 1 | 1 |
| CD28 dependent Vav1 pathway | R-HSA-389359 | 6.874354e-01 | 0.163 | 0 | 0 |
| Replication of the SARS-CoV-1 genome | R-HSA-9682706 | 6.874354e-01 | 0.163 | 0 | 0 |
| Impaired BRCA2 binding to RAD51 | R-HSA-9709570 | 6.903701e-01 | 0.161 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 6.903701e-01 | 0.161 | 0 | 0 |
| Negative regulation of FGFR4 signaling | R-HSA-5654733 | 6.903701e-01 | 0.161 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 6.904445e-01 | 0.161 | 0 | 0 |
| Collagen degradation | R-HSA-1442490 | 6.936687e-01 | 0.159 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 6.944421e-01 | 0.158 | 0 | 0 |
| Cholesterol biosynthesis | R-HSA-191273 | 6.992639e-01 | 0.155 | 0 | 0 |
| Signaling by FGFR3 | R-HSA-5654741 | 7.019023e-01 | 0.154 | 0 | 0 |
| NCAM signaling for neurite out-growth | R-HSA-375165 | 7.042439e-01 | 0.152 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 7.050335e-01 | 0.152 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 7.050335e-01 | 0.152 | 0 | 0 |
| Interleukin-37 signaling | R-HSA-9008059 | 7.050335e-01 | 0.152 | 0 | 0 |
| ERBB2 Activates PTK6 Signaling | R-HSA-8847993 | 7.081136e-01 | 0.150 | 0 | 0 |
| YAP1- and WWTR1 (TAZ)-stimulated gene expression | R-HSA-2032785 | 7.081136e-01 | 0.150 | 0 | 0 |
| Signaling by FGFR4 in disease | R-HSA-5655291 | 7.081136e-01 | 0.150 | 0 | 0 |
| HDL assembly | R-HSA-8963896 | 7.081136e-01 | 0.150 | 0 | 0 |
| P2Y receptors | R-HSA-417957 | 7.081136e-01 | 0.150 | 0 | 0 |
| SARS-CoV-1 Genome Replication and Transcription | R-HSA-9679514 | 7.081136e-01 | 0.150 | 0 | 0 |
| Diseases of DNA repair | R-HSA-9675135 | 7.137114e-01 | 0.146 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 7.175133e-01 | 0.144 | 0 | 0 |
| Signaling by FGFR2 | R-HSA-5654738 | 7.179170e-01 | 0.144 | 0 | 0 |
| PKR-mediated signaling | R-HSA-9833482 | 7.179170e-01 | 0.144 | 1 | 1 |
| MHC class II antigen presentation | R-HSA-2132295 | 7.183888e-01 | 0.144 | 0 | 0 |
| Respiratory syncytial virus (RSV) attachment and entry | R-HSA-9820960 | 7.191133e-01 | 0.143 | 0 | 0 |
| Budding and maturation of HIV virion | R-HSA-162588 | 7.191133e-01 | 0.143 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 7.197182e-01 | 0.143 | 1 | 0 |
| Insulin receptor signalling cascade | R-HSA-74751 | 7.245943e-01 | 0.140 | 0 | 0 |
| Beta-catenin phosphorylation cascade | R-HSA-196299 | 7.274251e-01 | 0.138 | 0 | 0 |
| ERBB2 Regulates Cell Motility | R-HSA-6785631 | 7.274251e-01 | 0.138 | 0 | 0 |
| Translesion synthesis by REV1 | R-HSA-110312 | 7.274251e-01 | 0.138 | 0 | 0 |
| Telomere C-strand synthesis initiation | R-HSA-174430 | 7.274251e-01 | 0.138 | 0 | 0 |
| Sema3A PAK dependent Axon repulsion | R-HSA-399954 | 7.274251e-01 | 0.138 | 0 | 0 |
| Signaling by PDGFRA extracellular domain mutants | R-HSA-9673770 | 7.274251e-01 | 0.138 | 0 | 0 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | R-HSA-9673767 | 7.274251e-01 | 0.138 | 0 | 0 |
| InlB-mediated entry of Listeria monocytogenes into host cell | R-HSA-8875360 | 7.274251e-01 | 0.138 | 0 | 0 |
| Activation of BAD and translocation to mitochondria | R-HSA-111447 | 7.274251e-01 | 0.138 | 0 | 0 |
| IRF3-mediated induction of type I IFN | R-HSA-3270619 | 7.274251e-01 | 0.138 | 0 | 0 |
| Developmental Lineage of Multipotent Pancreatic Progenitor Cells | R-HSA-9937080 | 7.326225e-01 | 0.135 | 0 | 0 |
| Downregulation of SMAD2/3:SMAD4 transcriptional activity | R-HSA-2173795 | 7.326225e-01 | 0.135 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 7.363644e-01 | 0.133 | 0 | 0 |
| Cytoprotection by HMOX1 | R-HSA-9707564 | 7.443268e-01 | 0.128 | 0 | 0 |
| Translesion synthesis by POLI | R-HSA-5656121 | 7.454599e-01 | 0.128 | 0 | 0 |
| Defective GALNT3 causes HFTC | R-HSA-5083625 | 7.454599e-01 | 0.128 | 0 | 0 |
| Defective GALNT12 causes CRCS1 | R-HSA-5083636 | 7.454599e-01 | 0.128 | 0 | 0 |
| TP53 Regulates Transcription of Caspase Activators and Caspases | R-HSA-6803207 | 7.454599e-01 | 0.128 | 0 | 0 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | R-HSA-399955 | 7.454599e-01 | 0.128 | 0 | 0 |
| Class I peroxisomal membrane protein import | R-HSA-9603798 | 7.454599e-01 | 0.128 | 0 | 0 |
| Fatty Acids bound to GPR40 (FFAR1) regulate insulin secretion | R-HSA-434316 | 7.454599e-01 | 0.128 | 0 | 0 |
| Regulation of glycolysis by fructose 2,6-bisphosphate metabolism | R-HSA-9634600 | 7.454599e-01 | 0.128 | 0 | 0 |
| Differentiation of T cells | R-HSA-9945266 | 7.454599e-01 | 0.128 | 0 | 0 |
| Differentiation of naive CD+ T cells to T helper 1 cells (Th1 cells) | R-HSA-9942503 | 7.454599e-01 | 0.128 | 0 | 0 |
| Regulation of NF-kappa B signaling | R-HSA-9758274 | 7.454599e-01 | 0.128 | 0 | 0 |
| Negative regulation of FLT3 | R-HSA-9706369 | 7.454599e-01 | 0.128 | 0 | 0 |
| HDR through Single Strand Annealing (SSA) | R-HSA-5685938 | 7.455748e-01 | 0.128 | 0 | 0 |
| G-protein beta:gamma signalling | R-HSA-397795 | 7.455748e-01 | 0.128 | 0 | 0 |
| Negative regulation of FGFR1 signaling | R-HSA-5654726 | 7.455748e-01 | 0.128 | 0 | 0 |
| p53-Dependent G1/S DNA damage checkpoint | R-HSA-69580 | 7.469657e-01 | 0.127 | 0 | 0 |
| p53-Dependent G1 DNA Damage Response | R-HSA-69563 | 7.469657e-01 | 0.127 | 0 | 0 |
| HDR through Homologous Recombination (HRR) | R-HSA-5685942 | 7.531360e-01 | 0.123 | 0 | 0 |
| Kidney development | R-HSA-9830369 | 7.531360e-01 | 0.123 | 0 | 0 |
| HCMV Late Events | R-HSA-9610379 | 7.559787e-01 | 0.121 | 0 | 0 |
| PI3K Cascade | R-HSA-109704 | 7.573407e-01 | 0.121 | 0 | 0 |
| Signaling by FGFR2 in disease | R-HSA-5655253 | 7.573407e-01 | 0.121 | 0 | 0 |
| NFE2L2 regulating anti-oxidant/detoxification enzymes | R-HSA-9818027 | 7.579849e-01 | 0.120 | 0 | 0 |
| EGR2 and SOX10-mediated initiation of Schwann cell myelination | R-HSA-9619665 | 7.579849e-01 | 0.120 | 0 | 0 |
| Effects of PIP2 hydrolysis | R-HSA-114508 | 7.579849e-01 | 0.120 | 0 | 0 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | R-HSA-9768727 | 7.579849e-01 | 0.120 | 0 | 0 |
| Meiosis | R-HSA-1500620 | 7.608928e-01 | 0.119 | 0 | 0 |
| Collagen biosynthesis and modifying enzymes | R-HSA-1650814 | 7.621281e-01 | 0.118 | 0 | 0 |
| G beta:gamma signalling through CDC42 | R-HSA-8964616 | 7.623025e-01 | 0.118 | 0 | 0 |
| Translesion synthesis by POLK | R-HSA-5655862 | 7.623025e-01 | 0.118 | 0 | 0 |
| TRAF6 mediated IRF7 activation in TLR7/8 or 9 signaling | R-HSA-975110 | 7.623025e-01 | 0.118 | 0 | 0 |
| SHC1 events in ERBB4 signaling | R-HSA-1250347 | 7.623025e-01 | 0.118 | 0 | 0 |
| STAT5 activation downstream of FLT3 ITD mutants | R-HSA-9702518 | 7.623025e-01 | 0.118 | 0 | 0 |
| Coenzyme A biosynthesis | R-HSA-196783 | 7.623025e-01 | 0.118 | 0 | 0 |
| Transcriptional regulation of testis differentiation | R-HSA-9690406 | 7.623025e-01 | 0.118 | 0 | 0 |
| RAB GEFs exchange GTP for GDP on RABs | R-HSA-8876198 | 7.688669e-01 | 0.114 | 0 | 0 |
| Defective homologous recombination repair (HRR) due to BRCA2 loss of function | R-HSA-9701190 | 7.698678e-01 | 0.114 | 0 | 0 |
| Negative regulation of FGFR2 signaling | R-HSA-5654727 | 7.698678e-01 | 0.114 | 0 | 0 |
| Diseases of DNA Double-Strand Break Repair | R-HSA-9675136 | 7.698678e-01 | 0.114 | 0 | 0 |
| Toll-like Receptor Cascades | R-HSA-168898 | 7.707284e-01 | 0.113 | 0 | 0 |
| Developmental Lineage of Pancreatic Ductal Cells | R-HSA-9925563 | 7.708635e-01 | 0.113 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 7.731492e-01 | 0.112 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 7.763218e-01 | 0.110 | 0 | 0 |
| RNA Polymerase I Promoter Escape | R-HSA-73772 | 7.770577e-01 | 0.110 | 0 | 0 |
| Defective C1GALT1C1 causes TNPS | R-HSA-5083632 | 7.780316e-01 | 0.109 | 0 | 0 |
| Synthesis of PIPs at the late endosome membrane | R-HSA-1660517 | 7.780316e-01 | 0.109 | 0 | 0 |
| PI3K events in ERBB2 signaling | R-HSA-1963642 | 7.780316e-01 | 0.109 | 0 | 0 |
| Glycogen storage diseases | R-HSA-3229121 | 7.780316e-01 | 0.109 | 0 | 0 |
| Elevation of cytosolic Ca2+ levels | R-HSA-139853 | 7.780316e-01 | 0.109 | 0 | 0 |
| Replication of the SARS-CoV-2 genome | R-HSA-9694686 | 7.780316e-01 | 0.109 | 0 | 0 |
| SCF-beta-TrCP mediated degradation of Emi1 | R-HSA-174113 | 7.812388e-01 | 0.107 | 0 | 0 |
| PERK regulates gene expression | R-HSA-381042 | 7.812388e-01 | 0.107 | 0 | 0 |
| Presynaptic phase of homologous DNA pairing and strand exchange | R-HSA-5693616 | 7.812388e-01 | 0.107 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 7.842051e-01 | 0.106 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 7.915730e-01 | 0.102 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 7.921137e-01 | 0.101 | 0 | 0 |
| Regulation of TP53 Degradation | R-HSA-6804757 | 7.921137e-01 | 0.101 | 1 | 1 |
| Lysosome Vesicle Biogenesis | R-HSA-432720 | 7.921137e-01 | 0.101 | 0 | 0 |
| Glycosphingolipid transport | R-HSA-9845576 | 7.921137e-01 | 0.101 | 0 | 0 |
| FGFR2 mutant receptor activation | R-HSA-1839126 | 7.921137e-01 | 0.101 | 0 | 0 |
| G beta:gamma signalling through PLC beta | R-HSA-418217 | 7.927207e-01 | 0.101 | 0 | 0 |
| Presynaptic function of Kainate receptors | R-HSA-500657 | 7.927207e-01 | 0.101 | 0 | 0 |
| RNA Polymerase III Transcription Termination | R-HSA-73980 | 7.927207e-01 | 0.101 | 0 | 0 |
| Chaperone Mediated Autophagy | R-HSA-9613829 | 7.927207e-01 | 0.101 | 0 | 0 |
| Organic anion transport by SLC5/17/25 transporters | R-HSA-428643 | 7.927207e-01 | 0.101 | 0 | 0 |
| Nucleotide-like (purinergic) receptors | R-HSA-418038 | 7.927207e-01 | 0.101 | 0 | 0 |
| Translation initiation complex formation | R-HSA-72649 | 7.954382e-01 | 0.099 | 0 | 0 |
| Base-Excision Repair, AP Site Formation | R-HSA-73929 | 7.954382e-01 | 0.099 | 0 | 0 |
| Voltage gated Potassium channels | R-HSA-1296072 | 8.025083e-01 | 0.096 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 8.027375e-01 | 0.095 | 1 | 1 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | R-HSA-1445148 | 8.033002e-01 | 0.095 | 0 | 0 |
| Pre-NOTCH Processing in Golgi | R-HSA-1912420 | 8.064386e-01 | 0.093 | 0 | 0 |
| Translesion Synthesis by POLH | R-HSA-110320 | 8.064386e-01 | 0.093 | 0 | 0 |
| Pyrimidine biosynthesis | R-HSA-500753 | 8.064386e-01 | 0.093 | 0 | 0 |
| Diseases of hemostasis | R-HSA-9671793 | 8.064386e-01 | 0.093 | 0 | 0 |
| Specification of the neural plate border | R-HSA-9834899 | 8.064386e-01 | 0.093 | 0 | 0 |
| STING mediated induction of host immune responses | R-HSA-1834941 | 8.064386e-01 | 0.093 | 0 | 0 |
| Strand-asynchronous mitochondrial DNA replication | R-HSA-9913635 | 8.064386e-01 | 0.093 | 0 | 0 |
| SARS-CoV-2 Genome Replication and Transcription | R-HSA-9694682 | 8.064386e-01 | 0.093 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 8.097843e-01 | 0.092 | 0 | 0 |
| Metabolism of nitric oxide: NOS3 activation and regulation | R-HSA-202131 | 8.124385e-01 | 0.090 | 0 | 0 |
| Purine salvage | R-HSA-74217 | 8.124385e-01 | 0.090 | 0 | 0 |
| Homologous DNA Pairing and Strand Exchange | R-HSA-5693579 | 8.124385e-01 | 0.090 | 0 | 0 |
| Ribosomal scanning and start codon recognition | R-HSA-72702 | 8.125356e-01 | 0.090 | 0 | 0 |
| Signaling by FGFR1 | R-HSA-5654736 | 8.125356e-01 | 0.090 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 8.153028e-01 | 0.089 | 0 | 0 |
| Glycogen synthesis | R-HSA-3322077 | 8.192494e-01 | 0.087 | 0 | 0 |
| Co-inhibition by CTLA4 | R-HSA-389513 | 8.192494e-01 | 0.087 | 0 | 0 |
| Signaling by NODAL | R-HSA-1181150 | 8.192494e-01 | 0.087 | 0 | 0 |
| Common Pathway of Fibrin Clot Formation | R-HSA-140875 | 8.192494e-01 | 0.087 | 0 | 0 |
| Protein hydroxylation | R-HSA-9629569 | 8.192494e-01 | 0.087 | 0 | 0 |
| Beta-catenin independent WNT signaling | R-HSA-3858494 | 8.197548e-01 | 0.086 | 0 | 0 |
| Antigen processing: Ubiquitination & Proteasome degradation | R-HSA-983168 | 8.205569e-01 | 0.086 | 0 | 0 |
| Protein folding | R-HSA-391251 | 8.254923e-01 | 0.083 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 8.257894e-01 | 0.083 | 0 | 0 |
| MyD88 deficiency (TLR2/4) | R-HSA-5602498 | 8.312130e-01 | 0.080 | 0 | 0 |
| NOTCH2 Activation and Transmission of Signal to the Nucleus | R-HSA-2979096 | 8.312130e-01 | 0.080 | 0 | 0 |
| SHC-mediated cascade:FGFR3 | R-HSA-5654704 | 8.312130e-01 | 0.080 | 0 | 0 |
| Acetylcholine Neurotransmitter Release Cycle | R-HSA-264642 | 8.312130e-01 | 0.080 | 0 | 0 |
| ERK/MAPK targets | R-HSA-198753 | 8.312130e-01 | 0.080 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 8.377473e-01 | 0.077 | 0 | 0 |
| Nuclear Receptor transcription pathway | R-HSA-383280 | 8.384940e-01 | 0.077 | 0 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 8.396016e-01 | 0.076 | 0 | 0 |
| Maturation of spike protein | R-HSA-9694548 | 8.396016e-01 | 0.076 | 0 | 0 |
| Unblocking of NMDA receptors, glutamate binding and activation | R-HSA-438066 | 8.423855e-01 | 0.074 | 0 | 0 |
| Ras activation upon Ca2+ influx through NMDA receptor | R-HSA-442982 | 8.423855e-01 | 0.074 | 0 | 0 |
| IRAK4 deficiency (TLR2/4) | R-HSA-5603041 | 8.423855e-01 | 0.074 | 0 | 0 |
| SHC-mediated cascade:FGFR4 | R-HSA-5654719 | 8.423855e-01 | 0.074 | 0 | 0 |
| Negative regulation of NMDA receptor-mediated neuronal transmission | R-HSA-9617324 | 8.423855e-01 | 0.074 | 0 | 0 |
| FRS-mediated FGFR3 signaling | R-HSA-5654706 | 8.423855e-01 | 0.074 | 0 | 0 |
| Molybdenum cofactor biosynthesis | R-HSA-947581 | 8.423855e-01 | 0.074 | 0 | 0 |
| Formation of paraxial mesoderm | R-HSA-9793380 | 8.500476e-01 | 0.071 | 0 | 0 |
| RAF-independent MAPK1/3 activation | R-HSA-112409 | 8.528190e-01 | 0.069 | 1 | 0 |
| FRS-mediated FGFR4 signaling | R-HSA-5654712 | 8.528190e-01 | 0.069 | 0 | 0 |
| NOTCH3 Activation and Transmission of Signal to the Nucleus | R-HSA-9013507 | 8.528190e-01 | 0.069 | 0 | 0 |
| Cholesterol biosynthesis via lathosterol | R-HSA-6807062 | 8.528190e-01 | 0.069 | 0 | 0 |
| COPI-dependent Golgi-to-ER retrograde traffic | R-HSA-6811434 | 8.547980e-01 | 0.068 | 0 | 0 |
| Termination of O-glycan biosynthesis | R-HSA-977068 | 8.625625e-01 | 0.064 | 0 | 0 |
| Prefoldin mediated transfer of substrate to CCT/TriC | R-HSA-389957 | 8.625625e-01 | 0.064 | 0 | 0 |
| Free fatty acids regulate insulin secretion | R-HSA-400451 | 8.625625e-01 | 0.064 | 0 | 0 |
| Carnitine shuttle | R-HSA-200425 | 8.625625e-01 | 0.064 | 0 | 0 |
| Synthesis of pyrophosphates in the cytosol | R-HSA-1855167 | 8.625625e-01 | 0.064 | 0 | 0 |
| Organic anion transport by SLCO transporters | R-HSA-879518 | 8.625625e-01 | 0.064 | 0 | 0 |
| Formation of the ureteric bud | R-HSA-9830674 | 8.625625e-01 | 0.064 | 0 | 0 |
| G1/S DNA Damage Checkpoints | R-HSA-69615 | 8.631190e-01 | 0.064 | 0 | 0 |
| Defective pyroptosis | R-HSA-9710421 | 8.631508e-01 | 0.064 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 8.631508e-01 | 0.064 | 0 | 0 |
| Signaling by FGFR | R-HSA-190236 | 8.653152e-01 | 0.063 | 0 | 0 |
| Translocation of ZAP-70 to Immunological synapse | R-HSA-202430 | 8.716615e-01 | 0.060 | 0 | 0 |
| TRAF6 mediated NF-kB activation | R-HSA-933542 | 8.716615e-01 | 0.060 | 0 | 0 |
| SHC-mediated cascade:FGFR1 | R-HSA-5654688 | 8.716615e-01 | 0.060 | 0 | 0 |
| Norepinephrine Neurotransmitter Release Cycle | R-HSA-181430 | 8.716615e-01 | 0.060 | 0 | 0 |
| ADP signalling through P2Y purinoceptor 1 | R-HSA-418592 | 8.716615e-01 | 0.060 | 0 | 0 |
| Plasma lipoprotein assembly | R-HSA-8963898 | 8.716615e-01 | 0.060 | 0 | 0 |
| Cellular response to hypoxia | R-HSA-1234174 | 8.751780e-01 | 0.058 | 0 | 0 |
| Fanconi Anemia Pathway | R-HSA-6783310 | 8.770434e-01 | 0.057 | 0 | 0 |
| DAG and IP3 signaling | R-HSA-1489509 | 8.770434e-01 | 0.057 | 0 | 0 |
| FRS-mediated FGFR1 signaling | R-HSA-5654693 | 8.801586e-01 | 0.055 | 0 | 0 |
| Defects in cobalamin (B12) metabolism | R-HSA-3296469 | 8.801586e-01 | 0.055 | 0 | 0 |
| Hyaluronan degradation | R-HSA-2160916 | 8.801586e-01 | 0.055 | 0 | 0 |
| Synthesis of PIPs at the early endosome membrane | R-HSA-1660516 | 8.801586e-01 | 0.055 | 0 | 0 |
| MicroRNA (miRNA) biogenesis | R-HSA-203927 | 8.801586e-01 | 0.055 | 0 | 0 |
| VEGFR2 mediated cell proliferation | R-HSA-5218921 | 8.801586e-01 | 0.055 | 0 | 0 |
| PIWI-interacting RNA (piRNA) biogenesis | R-HSA-5601884 | 8.801586e-01 | 0.055 | 0 | 0 |
| Formation of the nephric duct | R-HSA-9830364 | 8.801586e-01 | 0.055 | 0 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 8.827024e-01 | 0.054 | 0 | 0 |
| Formation of TC-NER Pre-Incision Complex | R-HSA-6781823 | 8.834909e-01 | 0.054 | 0 | 0 |
| SLC transporter disorders | R-HSA-5619102 | 8.844665e-01 | 0.053 | 0 | 0 |
| Glutamate Neurotransmitter Release Cycle | R-HSA-210500 | 8.880936e-01 | 0.052 | 0 | 0 |
| Metalloprotease DUBs | R-HSA-5689901 | 8.880936e-01 | 0.052 | 0 | 0 |
| Attachment of bacteria to epithelial cells | R-HSA-9638630 | 8.880936e-01 | 0.052 | 0 | 0 |
| Synthesis of IP2, IP, and Ins in the cytosol | R-HSA-1855183 | 8.880936e-01 | 0.052 | 0 | 0 |
| XBP1(S) activates chaperone genes | R-HSA-381038 | 8.885438e-01 | 0.051 | 0 | 0 |
| TAK1-dependent IKK and NF-kappa-B activation | R-HSA-445989 | 8.896242e-01 | 0.051 | 0 | 0 |
| Synthesis of PC | R-HSA-1483191 | 8.896242e-01 | 0.051 | 0 | 0 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | R-HSA-3371497 | 8.915013e-01 | 0.050 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 8.930863e-01 | 0.049 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 8.946510e-01 | 0.048 | 1 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 8.954566e-01 | 0.048 | 0 | 0 |
| Packaging Of Telomere Ends | R-HSA-171306 | 8.955036e-01 | 0.048 | 0 | 0 |
| Cobalamin (Cbl) metabolism | R-HSA-9759218 | 8.955036e-01 | 0.048 | 0 | 0 |
| Signaling by BMP | R-HSA-201451 | 8.955036e-01 | 0.048 | 0 | 0 |
| SHC-mediated cascade:FGFR2 | R-HSA-5654699 | 8.955036e-01 | 0.048 | 0 | 0 |
| RNA Polymerase I Promoter Opening | R-HSA-73728 | 8.955036e-01 | 0.048 | 0 | 0 |
| Mitochondrial unfolded protein response (UPRmt) | R-HSA-9841251 | 8.955036e-01 | 0.048 | 0 | 0 |
| Signaling by FGFR3 in disease | R-HSA-5655332 | 8.955036e-01 | 0.048 | 0 | 0 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | R-HSA-8866652 | 8.955036e-01 | 0.048 | 0 | 0 |
| Maturation of hRSV A proteins | R-HSA-9828806 | 8.955036e-01 | 0.048 | 0 | 0 |
| Nuclear events mediated by NFE2L2 | R-HSA-9759194 | 8.985664e-01 | 0.046 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 8.986016e-01 | 0.046 | 0 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 9.010011e-01 | 0.045 | 0 | 0 |
| COPII-mediated vesicle transport | R-HSA-204005 | 9.012937e-01 | 0.045 | 0 | 0 |
| Cytosolic sensors of pathogen-associated DNA | R-HSA-1834949 | 9.012937e-01 | 0.045 | 0 | 0 |
| Activation of AMPK downstream of NMDARs | R-HSA-9619483 | 9.024234e-01 | 0.045 | 0 | 0 |
| FRS-mediated FGFR2 signaling | R-HSA-5654700 | 9.024234e-01 | 0.045 | 0 | 0 |
| Activation of kainate receptors upon glutamate binding | R-HSA-451326 | 9.024234e-01 | 0.045 | 0 | 0 |
| ATF4 activates genes in response to endoplasmic reticulum stress | R-HSA-380994 | 9.024234e-01 | 0.045 | 0 | 0 |
| Pyrimidine salvage | R-HSA-73614 | 9.024234e-01 | 0.045 | 0 | 0 |
| Pyroptosis | R-HSA-5620971 | 9.024234e-01 | 0.045 | 0 | 0 |
| Inflammasomes | R-HSA-622312 | 9.024234e-01 | 0.045 | 0 | 0 |
| Unfolded Protein Response (UPR) | R-HSA-381119 | 9.076618e-01 | 0.042 | 0 | 0 |
| DNA methylation | R-HSA-5334118 | 9.088854e-01 | 0.041 | 0 | 0 |
| Late endosomal microautophagy | R-HSA-9615710 | 9.088854e-01 | 0.041 | 0 | 0 |
| Regulation of gene expression in beta cells | R-HSA-210745 | 9.088854e-01 | 0.041 | 0 | 0 |
| Platelet calcium homeostasis | R-HSA-418360 | 9.088854e-01 | 0.041 | 0 | 0 |
| Downstream signaling of activated FGFR3 | R-HSA-5654708 | 9.088854e-01 | 0.041 | 0 | 0 |
| Nitric oxide stimulates guanylate cyclase | R-HSA-392154 | 9.088854e-01 | 0.041 | 0 | 0 |
| Signaling by CSF3 (G-CSF) | R-HSA-9674555 | 9.088854e-01 | 0.041 | 0 | 0 |
| Meiotic recombination | R-HSA-912446 | 9.112761e-01 | 0.040 | 0 | 0 |
| IRE1alpha activates chaperones | R-HSA-381070 | 9.138536e-01 | 0.039 | 0 | 0 |
| DAP12 signaling | R-HSA-2424491 | 9.149197e-01 | 0.039 | 0 | 0 |
| Thrombin signalling through proteinase activated receptors (PARs) | R-HSA-456926 | 9.149197e-01 | 0.039 | 0 | 0 |
| Downstream signaling of activated FGFR4 | R-HSA-5654716 | 9.149197e-01 | 0.039 | 0 | 0 |
| Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | R-HSA-1474151 | 9.149197e-01 | 0.039 | 0 | 0 |
| Signaling by Insulin receptor | R-HSA-74752 | 9.175345e-01 | 0.037 | 0 | 0 |
| Plasma lipoprotein assembly, remodeling, and clearance | R-HSA-174824 | 9.175345e-01 | 0.037 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 9.191089e-01 | 0.037 | 0 | 0 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | R-HSA-389958 | 9.205548e-01 | 0.036 | 0 | 0 |
| Negative regulators of DDX58/IFIH1 signaling | R-HSA-936440 | 9.205548e-01 | 0.036 | 0 | 0 |
| Molecules associated with elastic fibres | R-HSA-2129379 | 9.205548e-01 | 0.036 | 0 | 0 |
| Cargo concentration in the ER | R-HSA-5694530 | 9.205548e-01 | 0.036 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 9.225682e-01 | 0.035 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 9.254369e-01 | 0.034 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 9.254369e-01 | 0.034 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected purine | R-HSA-110330 | 9.258170e-01 | 0.033 | 0 | 0 |
| G alpha (z) signalling events | R-HSA-418597 | 9.288959e-01 | 0.032 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 9.306167e-01 | 0.031 | 0 | 0 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | R-HSA-9668328 | 9.307309e-01 | 0.031 | 0 | 0 |
| CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling | R-HSA-442742 | 9.307309e-01 | 0.031 | 0 | 0 |
| Assembly of the ORC complex at the origin of replication | R-HSA-68616 | 9.307309e-01 | 0.031 | 0 | 0 |
| Resolution of D-loop Structures through Holliday Junction Intermediates | R-HSA-5693568 | 9.307309e-01 | 0.031 | 0 | 0 |
| Cardiogenesis | R-HSA-9733709 | 9.307309e-01 | 0.031 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 9.307309e-01 | 0.031 | 0 | 0 |
| Ion homeostasis | R-HSA-5578775 | 9.327537e-01 | 0.030 | 0 | 0 |
| PCP/CE pathway | R-HSA-4086400 | 9.329596e-01 | 0.030 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 9.329596e-01 | 0.030 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 9.349438e-01 | 0.029 | 0 | 0 |
| Acyl chain remodelling of PC | R-HSA-1482788 | 9.353196e-01 | 0.029 | 0 | 0 |
| Resolution of D-Loop Structures | R-HSA-5693537 | 9.353196e-01 | 0.029 | 0 | 0 |
| Vitamin B5 (pantothenate) metabolism | R-HSA-199220 | 9.353196e-01 | 0.029 | 0 | 0 |
| TP53 Regulates Metabolic Genes | R-HSA-5628897 | 9.367879e-01 | 0.028 | 0 | 0 |
| eNOS activation | R-HSA-203615 | 9.396045e-01 | 0.027 | 0 | 0 |
| Antigen Presentation: Folding, assembly and peptide loading of class I MHC | R-HSA-983170 | 9.396045e-01 | 0.027 | 0 | 0 |
| Autodegradation of the E3 ubiquitin ligase COP1 | R-HSA-349425 | 9.396045e-01 | 0.027 | 0 | 0 |
| Hyaluronan metabolism | R-HSA-2142845 | 9.396045e-01 | 0.027 | 0 | 0 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | R-HSA-6814122 | 9.396045e-01 | 0.027 | 0 | 0 |
| Regulation of TLR by endogenous ligand | R-HSA-5686938 | 9.396045e-01 | 0.027 | 0 | 0 |
| NOD1/2 Signaling Pathway | R-HSA-168638 | 9.396045e-01 | 0.027 | 0 | 0 |
| Signal amplification | R-HSA-392518 | 9.396045e-01 | 0.027 | 0 | 0 |
| NPAS4 regulates expression of target genes | R-HSA-9768919 | 9.396045e-01 | 0.027 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 9.418609e-01 | 0.026 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 9.418609e-01 | 0.026 | 0 | 0 |
| Amyloid fiber formation | R-HSA-977225 | 9.421997e-01 | 0.026 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 9.424187e-01 | 0.026 | 0 | 0 |
| Regulation of Apoptosis | R-HSA-169911 | 9.436059e-01 | 0.025 | 0 | 0 |
| Acyl chain remodelling of PE | R-HSA-1482839 | 9.436059e-01 | 0.025 | 0 | 0 |
| Downstream signaling of activated FGFR2 | R-HSA-5654696 | 9.436059e-01 | 0.025 | 0 | 0 |
| Downstream signaling of activated FGFR1 | R-HSA-5654687 | 9.436059e-01 | 0.025 | 0 | 0 |
| Defects in vitamin and cofactor metabolism | R-HSA-3296482 | 9.436059e-01 | 0.025 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 9.436059e-01 | 0.025 | 0 | 0 |
| Sphingolipid de novo biosynthesis | R-HSA-1660661 | 9.462894e-01 | 0.024 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 9.465421e-01 | 0.024 | 0 | 0 |
| Class I MHC mediated antigen processing & presentation | R-HSA-983169 | 9.472206e-01 | 0.024 | 0 | 0 |
| Interleukin-1 signaling | R-HSA-9020702 | 9.472775e-01 | 0.024 | 0 | 0 |
| PRC2 methylates histones and DNA | R-HSA-212300 | 9.473423e-01 | 0.023 | 0 | 0 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | R-HSA-450408 | 9.473423e-01 | 0.023 | 0 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 9.473423e-01 | 0.023 | 0 | 0 |
| Calmodulin induced events | R-HSA-111933 | 9.473423e-01 | 0.023 | 0 | 0 |
| CaM pathway | R-HSA-111997 | 9.473423e-01 | 0.023 | 0 | 0 |
| Formation of Fibrin Clot (Clotting Cascade) | R-HSA-140877 | 9.473423e-01 | 0.023 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 9.486918e-01 | 0.023 | 0 | 0 |
| PLC beta mediated events | R-HSA-112043 | 9.492437e-01 | 0.023 | 0 | 0 |
| Nucleotide salvage | R-HSA-8956321 | 9.492437e-01 | 0.023 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 9.505011e-01 | 0.022 | 0 | 0 |
| SIRT1 negatively regulates rRNA expression | R-HSA-427359 | 9.508315e-01 | 0.022 | 0 | 0 |
| Cleavage of the damaged purine | R-HSA-110331 | 9.508315e-01 | 0.022 | 0 | 0 |
| NCAM1 interactions | R-HSA-419037 | 9.508315e-01 | 0.022 | 0 | 0 |
| SLC-mediated transport of organic cations | R-HSA-549127 | 9.508315e-01 | 0.022 | 0 | 0 |
| tRNA processing in the mitochondrion | R-HSA-6785470 | 9.540896e-01 | 0.020 | 0 | 0 |
| Depurination | R-HSA-73927 | 9.540896e-01 | 0.020 | 0 | 0 |
| Elastic fibre formation | R-HSA-1566948 | 9.540896e-01 | 0.020 | 0 | 0 |
| Biofilm formation | R-HSA-9931953 | 9.540896e-01 | 0.020 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 9.540896e-01 | 0.020 | 0 | 0 |
| SLC-mediated transport of inorganic anions | R-HSA-9958790 | 9.540896e-01 | 0.020 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 9.547970e-01 | 0.020 | 0 | 0 |
| Stabilization of p53 | R-HSA-69541 | 9.571320e-01 | 0.019 | 0 | 0 |
| Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) | R-HSA-381771 | 9.571320e-01 | 0.019 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 9.571320e-01 | 0.019 | 0 | 0 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | R-HSA-168643 | 9.572040e-01 | 0.019 | 0 | 0 |
| Post NMDA receptor activation events | R-HSA-438064 | 9.593576e-01 | 0.018 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 9.595809e-01 | 0.018 | 0 | 0 |
| Glycogen metabolism | R-HSA-8982491 | 9.599729e-01 | 0.018 | 0 | 0 |
| Diseases associated with the TLR signaling cascade | R-HSA-5602358 | 9.599729e-01 | 0.018 | 0 | 0 |
| Diseases of Immune System | R-HSA-5260271 | 9.599729e-01 | 0.018 | 0 | 0 |
| rRNA processing in the mitochondrion | R-HSA-8868766 | 9.599729e-01 | 0.018 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 9.600329e-01 | 0.018 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 9.618580e-01 | 0.017 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 9.626258e-01 | 0.017 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 9.636056e-01 | 0.016 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 9.636056e-01 | 0.016 | 0 | 0 |
| Stimuli-sensing channels | R-HSA-2672351 | 9.636056e-01 | 0.016 | 0 | 0 |
| G-protein mediated events | R-HSA-112040 | 9.639605e-01 | 0.016 | 0 | 0 |
| Degradation of GLI1 by the proteasome | R-HSA-5610780 | 9.651029e-01 | 0.015 | 0 | 0 |
| Scavenging by Class A Receptors | R-HSA-3000480 | 9.651029e-01 | 0.015 | 0 | 0 |
| Assembly and cell surface presentation of NMDA receptors | R-HSA-9609736 | 9.651029e-01 | 0.015 | 0 | 0 |
| Neurotransmitter release cycle | R-HSA-112310 | 9.651369e-01 | 0.015 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 9.659757e-01 | 0.015 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 9.670391e-01 | 0.015 | 0 | 0 |
| Cytosolic tRNA aminoacylation | R-HSA-379716 | 9.674161e-01 | 0.014 | 0 | 0 |
| Ca-dependent events | R-HSA-111996 | 9.674161e-01 | 0.014 | 0 | 0 |
| Incretin synthesis, secretion, and inactivation | R-HSA-400508 | 9.674161e-01 | 0.014 | 0 | 0 |
| Response of Mtb to phagocytosis | R-HSA-9637690 | 9.695760e-01 | 0.013 | 0 | 0 |
| Fatty acyl-CoA biosynthesis | R-HSA-75105 | 9.696855e-01 | 0.013 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 9.698779e-01 | 0.013 | 0 | 0 |
| Diseases associated with O-glycosylation of proteins | R-HSA-3906995 | 9.713911e-01 | 0.013 | 0 | 0 |
| Cargo trafficking to the periciliary membrane | R-HSA-5620920 | 9.713911e-01 | 0.013 | 0 | 0 |
| ECM proteoglycans | R-HSA-3000178 | 9.713911e-01 | 0.013 | 0 | 0 |
| Metabolism of cofactors | R-HSA-8978934 | 9.713911e-01 | 0.013 | 0 | 0 |
| SCF(Skp2)-mediated degradation of p27/p21 | R-HSA-187577 | 9.715929e-01 | 0.013 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 9.715929e-01 | 0.013 | 0 | 0 |
| Cobalamin (Cbl, vitamin B12) transport and metabolism | R-HSA-196741 | 9.715929e-01 | 0.013 | 0 | 0 |
| Amine ligand-binding receptors | R-HSA-375280 | 9.715929e-01 | 0.013 | 0 | 0 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | R-HSA-2142691 | 9.715929e-01 | 0.013 | 0 | 0 |
| Surfactant metabolism | R-HSA-5683826 | 9.715929e-01 | 0.013 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 9.716449e-01 | 0.012 | 0 | 0 |
| Asymmetric localization of PCP proteins | R-HSA-4608870 | 9.734762e-01 | 0.012 | 0 | 0 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | R-HSA-168928 | 9.744501e-01 | 0.011 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 9.748482e-01 | 0.011 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 9.748482e-01 | 0.011 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 9.748482e-01 | 0.011 | 0 | 0 |
| Formation of the ternary complex, and subsequently, the 43S complex | R-HSA-72695 | 9.752347e-01 | 0.011 | 0 | 0 |
| Retrograde transport at the Trans-Golgi-Network | R-HSA-6811440 | 9.768767e-01 | 0.010 | 0 | 0 |
| Potassium Channels | R-HSA-1296071 | 9.769905e-01 | 0.010 | 0 | 0 |
| GPER1 signaling | R-HSA-9634597 | 9.784100e-01 | 0.009 | 0 | 0 |
| Metal ion SLC transporters | R-HSA-425410 | 9.784100e-01 | 0.009 | 0 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 9.786202e-01 | 0.009 | 0 | 0 |
| Translation of Structural Proteins | R-HSA-9694635 | 9.798367e-01 | 0.009 | 0 | 0 |
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | R-HSA-532668 | 9.798417e-01 | 0.009 | 0 | 0 |
| Chemokine receptors bind chemokines | R-HSA-380108 | 9.798417e-01 | 0.009 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 9.805605e-01 | 0.009 | 0 | 0 |
| SLC-mediated transport of organic anions | R-HSA-9955298 | 9.809860e-01 | 0.008 | 0 | 0 |
| Regulation of RAS by GAPs | R-HSA-5658442 | 9.811785e-01 | 0.008 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 9.811785e-01 | 0.008 | 0 | 0 |
| Interferon gamma signaling | R-HSA-877300 | 9.813861e-01 | 0.008 | 0 | 0 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | R-HSA-1234176 | 9.824267e-01 | 0.008 | 0 | 0 |
| Complex IV assembly | R-HSA-9864848 | 9.824267e-01 | 0.008 | 0 | 0 |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | R-HSA-9856530 | 9.830970e-01 | 0.007 | 0 | 0 |
| Activation of NMDA receptors and postsynaptic events | R-HSA-442755 | 9.832469e-01 | 0.007 | 0 | 0 |
| SARS-CoV-1 activates/modulates innate immune responses | R-HSA-9692916 | 9.835923e-01 | 0.007 | 0 | 0 |
| Transcriptional Regulation by NPAS4 | R-HSA-9634815 | 9.835923e-01 | 0.007 | 0 | 0 |
| Amino acids regulate mTORC1 | R-HSA-9639288 | 9.846806e-01 | 0.007 | 0 | 0 |
| Nucleotide biosynthesis | R-HSA-8956320 | 9.846806e-01 | 0.007 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 9.846806e-01 | 0.007 | 0 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 9.847249e-01 | 0.007 | 0 | 0 |
| Leishmania infection | R-HSA-9658195 | 9.847249e-01 | 0.007 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 9.849434e-01 | 0.007 | 0 | 0 |
| Paracetamol ADME | R-HSA-9753281 | 9.866456e-01 | 0.006 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 9.874613e-01 | 0.005 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 9.878295e-01 | 0.005 | 0 | 0 |
| Dectin-2 family | R-HSA-5621480 | 9.883587e-01 | 0.005 | 0 | 0 |
| Synthesis of PA | R-HSA-1483166 | 9.883587e-01 | 0.005 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 9.890490e-01 | 0.005 | 0 | 0 |
| Early SARS-CoV-2 Infection Events | R-HSA-9772572 | 9.891311e-01 | 0.005 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 9.894837e-01 | 0.005 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 9.895307e-01 | 0.005 | 0 | 0 |
| Peroxisomal protein import | R-HSA-9033241 | 9.898523e-01 | 0.004 | 0 | 0 |
| tRNA Aminoacylation | R-HSA-379724 | 9.905256e-01 | 0.004 | 0 | 0 |
| ER-Phagosome pathway | R-HSA-1236974 | 9.906686e-01 | 0.004 | 0 | 0 |
| Degradation of the extracellular matrix | R-HSA-1474228 | 9.907551e-01 | 0.004 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 9.916987e-01 | 0.004 | 0 | 0 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | R-HSA-8852276 | 9.917414e-01 | 0.004 | 1 | 1 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 9.922051e-01 | 0.003 | 0 | 0 |
| rRNA modification in the nucleus and cytosol | R-HSA-6790901 | 9.922895e-01 | 0.003 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 9.926600e-01 | 0.003 | 0 | 0 |
| Late SARS-CoV-2 Infection Events | R-HSA-9772573 | 9.926600e-01 | 0.003 | 0 | 0 |
| Glycerophospholipid biosynthesis | R-HSA-1483206 | 9.934602e-01 | 0.003 | 0 | 0 |
| tRNA modification in the nucleus and cytosol | R-HSA-6782315 | 9.937252e-01 | 0.003 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 9.938744e-01 | 0.003 | 0 | 0 |
| Disorders of transmembrane transporters | R-HSA-5619115 | 9.942380e-01 | 0.003 | 0 | 0 |
| O-linked glycosylation of mucins | R-HSA-913709 | 9.945307e-01 | 0.002 | 0 | 0 |
| Role of LAT2/NTAL/LAB on calcium mobilization | R-HSA-2730905 | 9.945722e-01 | 0.002 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 9.949639e-01 | 0.002 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 9.950935e-01 | 0.002 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 9.951919e-01 | 0.002 | 0 | 0 |
| Regulation of insulin secretion | R-HSA-422356 | 9.951919e-01 | 0.002 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 9.955239e-01 | 0.002 | 0 | 0 |
| Hedgehog 'on' state | R-HSA-5632684 | 9.955494e-01 | 0.002 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 9.955994e-01 | 0.002 | 0 | 0 |
| Formation of the cornified envelope | R-HSA-6809371 | 9.957249e-01 | 0.002 | 0 | 0 |
| Hedgehog 'off' state | R-HSA-5610787 | 9.957421e-01 | 0.002 | 0 | 0 |
| ABC-family proteins mediated transport | R-HSA-382556 | 9.957421e-01 | 0.002 | 0 | 0 |
| Neurotransmitter receptors and postsynaptic signal transmission | R-HSA-112314 | 9.958177e-01 | 0.002 | 0 | 0 |
| Interconversion of nucleotide di- and triphosphates | R-HSA-499943 | 9.958449e-01 | 0.002 | 0 | 0 |
| Diseases of carbohydrate metabolism | R-HSA-5663084 | 9.961208e-01 | 0.002 | 0 | 0 |
| ROS and RNS production in phagocytes | R-HSA-1222556 | 9.963785e-01 | 0.002 | 0 | 0 |
| Citric acid cycle (TCA cycle) | R-HSA-71403 | 9.966190e-01 | 0.001 | 0 | 0 |
| Opioid Signalling | R-HSA-111885 | 9.966634e-01 | 0.001 | 0 | 0 |
| Metabolism of steroids | R-HSA-8957322 | 9.969316e-01 | 0.001 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 9.970327e-01 | 0.001 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 9.972229e-01 | 0.001 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 9.973659e-01 | 0.001 | 1 | 0 |
| Antigen processing-Cross presentation | R-HSA-1236975 | 9.975435e-01 | 0.001 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 9.984039e-01 | 0.001 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 9.984129e-01 | 0.001 | 0 | 0 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | R-HSA-163841 | 9.985184e-01 | 0.001 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 9.987088e-01 | 0.001 | 0 | 0 |
| Downstream TCR signaling | R-HSA-202424 | 9.988748e-01 | 0.000 | 0 | 0 |
| Class B/2 (Secretin family receptors) | R-HSA-373080 | 9.988748e-01 | 0.000 | 0 | 0 |
| G alpha (q) signalling events | R-HSA-416476 | 9.989329e-01 | 0.000 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 9.989496e-01 | 0.000 | 0 | 0 |
| Neddylation | R-HSA-8951664 | 9.990759e-01 | 0.000 | 0 | 0 |
| FCGR activation | R-HSA-2029481 | 9.991455e-01 | 0.000 | 0 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 9.992942e-01 | 0.000 | 0 | 0 |
| Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | R-HSA-9954709 | 9.993049e-01 | 0.000 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 9.993049e-01 | 0.000 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 9.993049e-01 | 0.000 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 9.993511e-01 | 0.000 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 9.993513e-01 | 0.000 | 0 | 0 |
| Transmission across Chemical Synapses | R-HSA-112315 | 9.994526e-01 | 0.000 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 9.995156e-01 | 0.000 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 9.995401e-01 | 0.000 | 0 | 0 |
| Cardiac conduction | R-HSA-5576891 | 9.995408e-01 | 0.000 | 0 | 0 |
| Infectious disease | R-HSA-5663205 | 9.995463e-01 | 0.000 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 9.995876e-01 | 0.000 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 9.995992e-01 | 0.000 | 0 | 0 |
| Ion channel transport | R-HSA-983712 | 9.996257e-01 | 0.000 | 0 | 0 |
| Integration of energy metabolism | R-HSA-163685 | 9.996851e-01 | 0.000 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 9.997224e-01 | 0.000 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 9.997224e-01 | 0.000 | 0 | 0 |
| Antimicrobial peptides | R-HSA-6803157 | 9.997844e-01 | 0.000 | 0 | 0 |
| G alpha (s) signalling events | R-HSA-418555 | 9.997878e-01 | 0.000 | 0 | 0 |
| Disease | R-HSA-1643685 | 9.998054e-01 | 0.000 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 9.998574e-01 | 0.000 | 0 | 0 |
| Role of phospholipids in phagocytosis | R-HSA-2029485 | 9.998574e-01 | 0.000 | 0 | 0 |
| Peptide hormone metabolism | R-HSA-2980736 | 9.998758e-01 | 0.000 | 0 | 0 |
| Binding and Uptake of Ligands by Scavenger Receptors | R-HSA-2173782 | 9.998781e-01 | 0.000 | 0 | 0 |
| Infection with Mycobacterium tuberculosis | R-HSA-9635486 | 9.999057e-01 | 0.000 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 9.999331e-01 | 0.000 | 0 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 9.999377e-01 | 0.000 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 9.999501e-01 | 0.000 | 0 | 0 |
| Sensory perception of taste | R-HSA-9717189 | 9.999588e-01 | 0.000 | 0 | 0 |
| Metabolism of carbohydrates and carbohydrate derivatives | R-HSA-71387 | 9.999726e-01 | 0.000 | 0 | 0 |
| O-linked glycosylation | R-HSA-5173105 | 9.999746e-01 | 0.000 | 0 | 0 |
| Keratinization | R-HSA-6805567 | 9.999757e-01 | 0.000 | 0 | 0 |
| Metabolism of nucleotides | R-HSA-15869 | 9.999758e-01 | 0.000 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 9.999849e-01 | 0.000 | 0 | 0 |
| Diseases of glycosylation | R-HSA-3781865 | 9.999871e-01 | 0.000 | 0 | 0 |
| Translation | R-HSA-72766 | 9.999892e-01 | 0.000 | 0 | 0 |
| Arachidonate metabolism | R-HSA-2142753 | 9.999916e-01 | 0.000 | 0 | 0 |
| Immune System | R-HSA-168256 | 9.999929e-01 | 0.000 | 1 | 0 |
| Metabolism of water-soluble vitamins and cofactors | R-HSA-196849 | 9.999944e-01 | 0.000 | 0 | 0 |
| Sphingolipid metabolism | R-HSA-428157 | 9.999957e-01 | 0.000 | 0 | 0 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 9.999982e-01 | 0.000 | 0 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 9.999982e-01 | 0.000 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 9.999982e-01 | 0.000 | 0 | 0 |
| Respiratory electron transport | R-HSA-611105 | 9.999987e-01 | 0.000 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 9.999992e-01 | 0.000 | 0 | 0 |
| Peptide ligand-binding receptors | R-HSA-375276 | 9.999993e-01 | 0.000 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 9.999994e-01 | 0.000 | 0 | 0 |
| Glycosaminoglycan metabolism | R-HSA-1630316 | 9.999995e-01 | 0.000 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 9.999997e-01 | 0.000 | 0 | 0 |
| Infection with Enterobacteria | R-HSA-9640148 | 9.999998e-01 | 0.000 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 9.999999e-01 | 0.000 | 0 | 0 |
| Metabolism of vitamins and cofactors | R-HSA-196854 | 9.999999e-01 | 0.000 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 1.000000e+00 | 0.000 | 1 | 0 |
| SLC-mediated transmembrane transport | R-HSA-425407 | 1.000000e+00 | 0.000 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 1.000000e+00 | 0.000 | 0 | 0 |
| G alpha (i) signalling events | R-HSA-418594 | 1.000000e+00 | 0.000 | 0 | 0 |
| Aerobic respiration and respiratory electron transport | R-HSA-1428517 | 1.000000e+00 | 0.000 | 0 | 0 |
| Diseases of metabolism | R-HSA-5668914 | 1.000000e+00 | 0.000 | 0 | 0 |
| Class A/1 (Rhodopsin-like receptors) | R-HSA-373076 | 1.000000e+00 | 0.000 | 0 | 0 |
| Fatty acid metabolism | R-HSA-8978868 | 1.000000e+00 | 0.000 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 1.000000e+00 | 0.000 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 1.000000e+00 | 0.000 | 0 | 0 |
| GPCR ligand binding | R-HSA-500792 | 1.000000e+00 | 0.000 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 1.000000e+00 | -0.000 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 1.000000e+00 | -0.000 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 1.000000e+00 | -0.000 | 0 | 0 |
| E2F-enabled inhibition of pre-replication complex formation | R-HSA-113507 | 1.000000e+00 | 0.000 | 1 | 1 |
| MASTL Facilitates Mitotic Progression | R-HSA-2465910 | 1.000000e+00 | 0.000 | 1 | 1 |
| Activation of NIMA Kinases NEK9, NEK6, NEK7 | R-HSA-2980767 | 1.000000e+00 | 0.000 | 1 | 1 |