Defective ABCA1 causes TGD
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Homo sapiens (human)
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Surfactant metabolism
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- ABC3
- ABCA3
- ADA2
- ADGF
- ADGRF5
- ADORA2
- ADORA2A
- ADORA2B
- ADRA2A
- ADRA2C
- ADRA2L2
- ADRA2R
- ADRA2RL2
- ADRAR
- BR22
- CCDC59
- CECR1
- CKAP4
- COLEC4
- COLEC5
- COLEC7
- CPSB
- CSF2R
- CSF2RA
- CSF2RB
- CSF2RY
- CTSH
- DMBT1
- GATA6
- GP340
- GPR116
- IDGFL
- IL3RB
- IL5RB
- KIAA0758
- LMCD1
- NAP1
- NAPA
- NAPSA
- NPT2
- P2RU1
- P2RY2
- PGA3
- PGA4
- PGA5
- PSAP
- PSPD
- REAM
- REC
- SFTA3
- SFTP1
- SFTP2
- SFTP3
- SFTP4
- SFTPA
- SFTPA1
- SFTPA1B
- SFTPA2
- SFTPA2B
- SFTPB
- SFTPC
- SFTPD
- SFTPH
- SLC17A2
- SLC34A1
- SLC34A2
- TAP26
- TTF1
- ZDHHC2
- ZNF372
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Homo sapiens (human)
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Defective CFTR causes cystic fibrosis
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- ABCC7
- C10orf69
- C22orf14
- C2orf30
- C7orf76
- C8orf2
- CFTR
- DER1
- DER2
- DER3
- DERL1
- DERL2
- DERL3
- DSS1
- ERLEC1
- ERLIN1
- ERLIN2
- FLANA
- G16
- HC2
- HC3
- HC8
- HC9
- HEL-220
- HEL-S-70
- HSPC
- IFI5111
- KE04
- KEO4
- KIAA0072
- KIAA0077
- KIAA0107
- LLN2
- LMP10
- LMP2
- LMP7
- LMPX
- LMPY
- MB1
- MCB1
- MECL1
- MIP224
- MOV34L
- MSS1
- NG2
- NU
- OS9
- PFAAP4
- POH1
- PROS26
- PROS27
- PROS30
- PSC2
- PSC3
- PSC5
- PSC8
- PSC9
- PSMA1
- PSMA2
- PSMA3
- PSMA4
- PSMA5
- PSMA6
- PSMA7
- PSMA7L
- PSMA8
- PSMB1
- PSMB10
- PSMB11
- PSMB2
- PSMB3
- PSMB4
- PSMB5
- PSMB5i
- PSMB6
- PSMB6i
- PSMB7
- PSMB8
- PSMB9
- PSMC1
- PSMC2
- PSMC3
- PSMC4
- PSMC5
- PSMC6
- PSMD1
- PSMD10
- PSMD11
- PSMD12
- PSMD13
- PSMD14
- PSMD2
- PSMD3
- PSMD4
- PSMD5
- PSMD6
- PSMD7
- PSMD8
- PSMD9
- PSME1
- PSME2
- PSME3
- PSME4
- PSMF1
- RING10
- RING12
- RMA1
- RNF185
- RNF5
- RPS27A
- SEL1L
- SEM1
- SHFDG1
- SHFM1
- SPFH1
- SPFH2
- SUG1
- SUG2
- TBP1
- TBP7
- TRAP2
- TSA305
- UBA52
- UBA80
- UBB
- UBC
- UBCEP1
- UBCEP2
- VCP
- X
- XTP3TPB
- Y
- Y2
- Z
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Homo sapiens (human)
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Defective SLC40A1 causes hemochromatosis 4 (HFE4) (duodenum)
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- FPN
- FPN1
- HEPH
- IREG1
- KIAA0698
- SLC11A3
- SLC40A1
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Homo sapiens (human)
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MET interacts with TNS proteins
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- CTEN
- FNRB
- HGF
- HPTA
- ITGB1
- MDF2
- MET
- MSK12
- TEM6
- TENS1
- TNS3
- TNS4
- TPP
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Homo sapiens (human)
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PI-3K cascade:FGFR4
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- FGF1
- FGF16
- FGF18
- FGF19
- FGF2
- FGF20
- FGF23
- FGF4
- FGF6
- FGF9
- FGFA
- FGFB
- FGFR4
- FRS2
- GAB1
- GRB1
- HST
- HST2
- HSTF1
- HSTF2
- HYPF
- JTK2
- KLB
- KS3
- PIK3CA
- PIK3R1
- PTP2C
- PTPN11
- SHPTP2
- TKF
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Homo sapiens (human)
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Role of second messengers in netrin-1 signaling
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- DCC
- IGDCC1
- NTN1
- NTN1L
- PITPN
- PITPNA
- PLC1
- PLCG1
- TRP1
- TRP3
- TRP5
- TRP6
- TRP7
- TRPC1
- TRPC3
- TRPC4
- TRPC5
- TRPC6
- TRPC7
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Homo sapiens (human)
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Synthesis of UDP-N-acetyl-glucosamine
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- AGM1
- AMDHD2
- GFAT
- GFPT
- GFPT1
- GFPT2
- GNA1
- GNPNAT1
- NAGK
- PGM3
- RENBP
- SPAG2
- UAP1
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Homo sapiens (human)
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LXRs regulate gene expression linked to lipogenesis
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- ANGPT5
- ANGPTL3
- FADS5
- FAS
- FASN
- LXRA
- LXRB
- NER
- NR1H2
- NR1H3
- NR2B1
- NR2B2
- NRIP1
- RXRA
- RXRB
- SCD
- SCD1
- SCDOS
- UNR
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Homo sapiens (human)
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G beta:gamma signalling through CDC42
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- ARHGEF6
- CDC42
- COOL2
- GNB1
- GNB2
- GNB3
- GNB4
- GNB5
- GNG10
- GNG11
- GNG12
- GNG13
- GNG2
- GNG3
- GNG4
- GNG5
- GNG7
- GNG8
- GNG9
- GNGT1
- GNGT10
- GNGT11
- GNGT2
- GNGT3
- GNGT4
- GNGT5
- GNGT7
- GNGT8
- GNGT9
- KIAA0006
- PAK1
- PIXA
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Homo sapiens (human)
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Defective SLC22A5 causes systemic primary carnitine deficiency (CDSP)
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Homo sapiens (human)
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TRIF-mediated programmed cell death
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- CASP8
- CD14
- ESOP1
- FADD
- LY96
- MCH5
- MD2
- MORT1
- PRVTIRB
- RIP
- RIP1
- RIP3
- RIPK1
- RIPK3
- TICAM1
- TICAM2
- TIRAP3
- TIRP
- TLR4
- TRAM
- TRIF
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Homo sapiens (human)
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Processive synthesis on the C-strand of the telomere
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- ACD
- BLM
- DRIP5
- KIAA0039
- LIG1
- PCNA
- PIN2
- PIP1
- POLD
- POLD1
- POLD2
- POLD3
- POLD4
- POLDS
- POT1
- PTOP
- RAP1
- RECQ2
- RECQ3
- RECQL2
- RECQL3
- TERF1
- TERF2
- TERF2IP
- TIN2
- TINF2
- TINT1
- TPP1
- TRBF1
- TRBF2
- TRF
- TRF1
- TRF2
- WRN
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Homo sapiens (human)
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Defective ABCB11 causes PFIC2 and BRIC2
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Homo sapiens (human)
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Signal transduction by L1
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- CAML1
- CK2A1
- CK2A2
- CK2N
- CSNK2A1
- CSNK2A2
- CSNK2B
- EGFR
- ERBB
- ERBB1
- ERK1
- ERK2
- FNRA
- FNRB
- G5A
- GP2B
- GP3A
- HER1
- ITGA2B
- ITGA5
- ITGA9
- ITGAB
- ITGAV
- ITGB1
- ITGB3
- L1CAM
- MAP2K1
- MAP2K2
- MAPK1
- MAPK3
- MDF2
- MEK1
- MEK2
- MIC5
- MKK2
- MSK12
- MSK8
- NCAM
- NCAM1
- NRP
- NRP1
- PAK1
- PRKM1
- PRKM2
- PRKM3
- PRKMK1
- PRKMK2
- RAC1
- TC25
- VAV2
- VEGF165R
- VNRA
- VTNR
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Homo sapiens (human)
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Alpha-oxidation of phytanate
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- ACSVL1
- FACVL1
- FATP2
- HACL1
- HPCL
- HPCL2
- PAHX
- PECR
- PHYH
- PHYH2
- PMP34
- SDR29C1
- SLC25A17
- SLC27A2
- VLACS
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Homo sapiens (human)
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Signaling by activated point mutants of FGFR3
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- FGF1
- FGF16
- FGF18
- FGF2
- FGF20
- FGF23
- FGF4
- FGF9
- FGFA
- FGFB
- FGFR3
- HST
- HSTF1
- HYPF
- JTK4
- KS3
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Homo sapiens (human)
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Signaling by LTK
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- ACK1
- ALKAL1
- ALKAL2
- ASH
- FAM150A
- FAM150B
- GRB1
- GRB2
- IRS1
- LTK
- PIK3C1
- PIK3CA
- PIK3CB
- PIK3R1
- PIK3R2
- SOS1
- TNK2
- TYK1
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Homo sapiens (human)
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Defective TBXAS1 causes GHDD
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Homo sapiens (human)
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mRNA decay by 5' to 3' exoribonuclease
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- C6orf28
- CASM
- DCP1A
- DCP1B
- DCP2
- DDX6
- EDC3
- EDC4
- G7B
- HEDLS
- HLR2
- LSM1
- LSM16
- LSM2
- LSM3
- LSM4
- LSM5
- LSM6
- LSM7
- NUDT20
- PATL1
- RCK
- SEP1
- SMIF
- XRN1
- YJDC
- YJEFN2
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Homo sapiens (human)
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IRE1alpha activates chaperones
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Homo sapiens (human)
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Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants
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- APRF
- FYN
- GRB1
- HRAS
- HRAS1
- JAK2
- JTK8
- KIT
- LCK
- LYN
- NRAS
- PIK3CA
- PIK3R1
- PIK3R2
- PIK3R3
- SCFR
- SOS1
- STAT1
- STAT3
- STAT5
- STAT5A
- STAT5B
- YES
- YES1
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Homo sapiens (human)
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Regulation of TP53 Degradation
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- AKT1
- AKT2
- AKT3
- ATM
- BING2
- C20orf104
- CCN1
- CCNA
- CCNA1
- CCNA2
- CCNG
- CCNG1
- CDC2
- CDC28A
- CDK1
- CDK2
- CDKN1
- CDKN2
- CDKN2A
- CDS1
- CHEK2
- CHK2
- CYCG1
- DAP6
- DAXX
- FRAP
- FRAP1
- FRAP2
- GBL
- GLEA2
- HAUSP
- HCA58
- KIAA0044
- KIAA1999
- LST8
- MAPKAP1
- MDM2
- MDM4
- MDMX
- MIP1
- MLM
- MLST8
- MTOR
- NZF
- P34CDC2
- P53
- PDK1
- PDPK1
- PHF20
- PKB
- PKBG
- PPP2CA
- PPP2CB
- PPP2R1A
- PPP2R1B
- PPP2R5C
- PROTOR1
- PRR5
- RAC
- RAD53
- RAFT1
- RAPT1
- RFFL
- RICTOR
- RNF189
- RNF34
- RNF34L
- RPS27A
- SGK
- SGK1
- SIN1
- TP53
- TZP
- UBA52
- UBA80
- UBB
- UBC
- UBCEP1
- UBCEP2
- UBP41
- USP2
- USP7
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Homo sapiens (human)
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RUNX3 regulates RUNX1-mediated transcription
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- AML2
- CBFA3
- CBFB
- PEBP2A3
- RUNX3
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Homo sapiens (human)
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PLCG1 events in ERBB2 signaling
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- EGF
- EGFR
- ERBB
- ERBB1
- ERBB2
- HER1
- HER2
- MLN19
- NEU
- NGL
- PLC1
- PLCG1
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Homo sapiens (human)
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