Synthesis of PIPs at the Golgi membrane
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|
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- ARF1
- ARF3
- FIG4
- INPP5E
- KIAA0274
- KIAA0851
- KIAA0981
- OCRL
- OCRL1
- PI4K2A
- PI4K2B
- PI4KA
- PI4KB
- PIK3C2A
- PIK3C2G
- PIK3C3
- PIK3R4
- PIK4
- PIK4CA
- PIK4CB
- PIKFYVE
- PIP5K3
- SAC1
- SAC3
- SACM1L
- TAX1BP2
- TPIP
- TPTE
- TPTE2
- TRX
- VAC14
- VPS15
- VPS34
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Homo sapiens (human)
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|
Membrane binding and targetting of GAG proteins
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|
|
- C9orf28
- CFBP
- FAM125A
- FAM125B
- HCRP1
- MVB12A
- MVB12B
- NMT2
- PML39
- RPS27A
- TSG101
- UBA52
- UBA80
- UBAP1
- UBB
- UBC
- UBCEP1
- UBCEP2
- VPS28
- VPS37A
- VPS37B
- VPS37C
- VPS37D
- WBSCR24
- gag
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Homo sapiens (human)
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Defective SLC7A7 causes lysinuric protein intolerance (LPI)
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Homo sapiens (human)
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|
PERK regulates gene expression
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|
- ATF4
- CREB2
- EIF2A
- EIF2AK3
- EIF2B
- EIF2G
- EIF2S1
- EIF2S2
- EIF2S3
- GRP78
- HSPA5
- PEK
- PERK
- TXREB
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Homo sapiens (human)
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Defective CD320 causes MMATC
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|
|
|
Homo sapiens (human)
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Retrograde neurotrophin signalling
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|
- ADTAA
- ADTAB
- ADTB2
- AP17
- AP2A1
- AP2A2
- AP2B1
- AP2M1
- AP2S1
- CLAPA1
- CLAPA2
- CLAPB1
- CLAPM1
- CLAPS2
- CLH17
- CLTA
- CLTC
- CLTCL2
- CNSA2
- DNAL4
- DNM
- DNM1
- DNM2
- DNM3
- DYN2
- HIP9
- HYPJ
- KIAA0034
- KIAA0109
- KIAA0820
- KIAA0899
- MTC
- NGF
- NGFB
- NTRK1
- SH3D2A
- SH3GL2
- TRK
- TRKA
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Homo sapiens (human)
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Defective SLC6A19 causes Hartnup disorder (HND)
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|
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|
Homo sapiens (human)
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TNFR1-induced proapoptotic signaling
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|
|
- API1
- API2
- API3
- BIRC2
- BIRC3
- BIRC4
- C20orf18
- CASP8
- CYLD
- CYLD1
- DUBA7
- FADD
- FIP2
- GLC1E
- HIP7
- HYPL
- IAP3
- IKBKE
- IKKE
- IKKI
- KIAA0151
- KIAA0757
- KIAA0849
- MCH5
- MIB2
- MIHB
- MIHC
- MORT1
- NAK
- NRP
- OPTN
- OTDC1
- OTUD1
- OTUD7B
- OTUD7C
- PD1
- RBCK1
- RIP
- RIP1
- RIPK1
- RNF31
- RNF48
- RNF49
- RNF54
- SHARPIN
- SIPL1
- SKD
- SPATA2
- TBK1
- TNF
- TNFA
- TNFAIP3
- TNFAR
- TNFR1
- TNFRSF1A
- TNFSF2
- TRADD
- TRAF2
- TRAP3
- UBCE7IP3
- UBP41
- UL36
- UNP
- UNPH
- USP2
- USP21
- USP23
- USP4
- XAP3
- XAP4
- XIAP
- ZA20D1
- ZIBRA
- ZZANK1
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Homo sapiens (human)
|
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Regulation of localization of FOXO transcription factors
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- AFX
- AFX1
- AKT1
- AKT2
- AKT3
- FKHR
- FKHRL1
- FOXO1
- FOXO1A
- FOXO3
- FOXO3A
- FOXO4
- FOXO6
- HME1
- MLLT7
- PKB
- PKBG
- RAC
- SFN
- YWHAB
- YWHAG
- YWHAQ
- YWHAZ
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Homo sapiens (human)
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|
Metabolism of Angiotensinogen to Angiotensins
|
|
|
- ACE
- ACE2
- AGT
- ANPEP
- APN
- ATP6AP2
- ATP6IP2
- CAPER
- CD13
- CES1
- CES2
- CGL2
- CMA1
- CPA3
- CPB
- CPB1
- CPB2
- CPSD
- CTSD
- CTSG
- CTSGL2
- CTSZ
- CYH
- CYM
- DCP
- DCP1
- ELDF10
- ENPEP
- EPN
- GZMH
- MME
- PCPB
- PEPN
- REN
- SERPINA8
- SES1
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Homo sapiens (human)
|
|
Factors involved in megakaryocyte development and platelet production
|
|
|
- ABL
- ABL1
- AK3
- AK3L1
- AK6
- AKAP1
- AKAP10
- AKAP149
- AKL3L
- AOF2
- APS
- BHC80
- BRAF35
- C20orf150
- CABLES
- CABLES1
- CABLES2
- CAPZA1
- CAPZA2
- CAPZB
- CARMIL
- CARMIL1
- CBX5
- CDC42
- CDK2
- CDK5
- CDKN2
- CDKN5
- CPRP1
- DOCK1
- DOCK10
- DOCK11
- DOCK2
- DOCK3
- DOCK4
- DOCK5
- DOCK6
- DOCK7
- DOCK8
- DOCK9
- EHD1
- EHD2
- EHD3
- ERYF1
- FOG1
- FOG2
- GATA1
- GATA2
- GATA3
- GATA4
- GATA5
- GATA6
- GF1
- H3-3A
- H3-3B
- H3.3A
- H3.3B
- H3C1
- H3C10
- H3C11
- H3C12
- H3C13
- H3C14
- H3C15
- H3C2
- H3C3
- H3C4
- H3C6
- H3C7
- H3C8
- H3F2
- H3F3
- H3F3A
- H3F3B
- H3FA
- H3FB
- H3FC HIST1H3C
- H3FD
- H3FF
- H3FH
- H3FI
- H3FJ
- H3FK
- H3FL
- H3FM
- HBB
- HBD
- HBE
- HBE1
- HBG1
- HBG2
- HDAC1
- HDAC2
- HIST1H3A
- HIST1H3B
- HIST1H3D
- HIST1H3E
- HIST1H3F
- HIST1H3G
- HIST1H3H
- HIST1H3I
- HIST1H3J
- HIST2H3A
- HIST2H3C
- HIST2H3D
- HMG20B
- HMGX2
- HMGXB2
- HP1A
- IFB
- IFNA1
- IFNA10
- IFNA13
- IFNA14
- IFNA16
- IFNA17
- IFNA2
- IFNA21
- IFNA2A
- IFNA2B
- IFNA2C
- IFNA4
- IFNA5
- IFNA6
- IFNA7
- IFNA8
- IFNB
- IFNB1
- IRF1
- IRF2
- ITPK1
- JAK2
- JHDM2C
- JMJD1C
- JTK7
- KDM1
- KDM1A
- KIAA0071
- KIAA0209
- KIAA0214
- KIAA0299
- KIAA0601
- KIAA0694
- KIAA0716
- KIAA1058
- KIAA1299
- KIAA1380
- KIAA1395
- KIAA1696
- KIAA1771
- LNK
- LRRC16
- LRRC16A
- LSD1
- MAFF
- MAFG
- MAFK
- MFN1
- MFN2
- MICAL
- MICAL1
- MOCA
- MYB
- NFE2
- NICAL
- P53
- PAST
- PAST1
- PAST2
- PAST3
- PHF21A
- PKACA
- PKR1
- PKR2
- PRKA1
- PRKACA
- PRKACB
- PRKACG
- PRKAR1
- PRKAR1A
- PRKAR1B
- PRKAR2
- PRKAR2A
- PRKAR2B
- PSSALRE
- RAB5
- RAB5A
- RAC1
- RAD51B
- RAD51C
- RAD51L1
- RAD51L2
- RBSN
- RCOR
- RCOR1
- REC2
- RPD3L1
- SH2B
- SH2B1
- SH2B2
- SH2B3
- SIN3A
- SMARCE1R
- TC25
- TP53
- TRIP8
- TSE1
- VPS45
- VPS45A
- VPS45B
- WEE1
- ZFN89A
- ZFPM1
- ZFPM2
- ZFYVE20
- ZIZ1
- ZIZ2
- ZIZ3
- ZNF89B
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Homo sapiens (human)
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|
Defective CHST14 causes EDS, musculocontractural type
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|
|
- BCAN
- BEHAB
- BGN
- CALEB
- CHST14
- CSPG2
- CSPG3
- CSPG4
- CSPG5
- CSPG7
- D4ST1
- DCN
- MCSP
- NCAN
- NEUR
- NGC
- SLRR1A
- SLRR1B
- VCAN
|
Homo sapiens (human)
|
|
Post-translational modification: synthesis of GPI-anchored proteins
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|
|
- 9804
- ALPG
- ALPI
- ALPL
- ALPPL
- ALPPL2
- ART3
- ART4
- BST1
- C11orf34
- C4.4A
- C6orf23
- C6orf24
- CD109
- CD16B
- CD52
- CDW52
- CEA
- CEACAM5
- CEACAM7
- CGM2
- CNTN3
- CNTN4
- CNTN5
- CO16
- CPAMD7
- CPM
- DO
- DOK1
- DPL
- E48
- ESP1
- FCG3
- FCGR3
- FCGR3B
- FOLR2
- FOLR4
- G6C
- G6D
- GP2
- GPIHBP1
- GPLD1
- HBP1
- HE5
- IGFR3
- IGLON1
- IGLON2
- IGLON3
- IGLON4
- IZUMO1R
- JUNO
- KIAA0976
- KIAA1496
- KIAA1857
- LAMP
- LMNT1
- LMNT2
- LSAMP
- LY6D
- LY6E
- LY6G6C
- LY6G6D
- LY6H
- LY6K
- LYPD1
- LYPD2
- LYPD3
- LYPD4
- LYPD5
- LYPD6B
- LYPD8
- LYPDC1
- LYPDC2
- Lynx2
- MAMDC1
- MAMDC3
- MAP97
- MDGA1
- MDGA2
- MEGT1
- MELTF
- MFI2
- MPF
- MSLN
- N2DL2
- NEGR1
- NG24
- NG25
- NGRH1
- NGRH2
- NGRL2
- NGRL3
- NRN
- NRN1
- NRN1L
- NT
- NTM
- NTNG1
- NTNG2
- OBCAM
- OPCML
- OTOA
- PANG
- PIGPLD1
- PLET1
- PRND
- PRSS21
- PRSS41
- PSCA
- RAET1G
- RAET1H
- RAET1L
- RECK
- RIGE
- RTN4RL1
- RTN4RL2
- SAMP14
- SCA2
- SGRG
- SHO
- SPACA4
- SPRN
- ST15
- TECTA
- TECTB
- TESSP1
- TEST1
- TEX101
- THY1
- TMART
- TSA1
- ULBP2
- ULBP5
- ULBP6
- VNN1
- VNN2
- XPNPEP2
|
Homo sapiens (human)
|
|
NCAM1 interactions
|
|
|
- AGRIN
- AGRN
- ALTPRP
- ARTN
- AXT
- CACH1
- CACH2
- CACH3
- CACN1
- CACN2
- CACN4
- CACNA1C
- CACNA1D
- CACNA1G
- CACNA1H
- CACNA1I
- CACNA1S
- CACNB1
- CACNB2
- CACNB3
- CACNB4
- CACNL1A1
- CACNL1A2
- CACNL1A3
- CACNLB1
- CACNLB2
- CACNLB3
- CACNLB4
- CCHL1A1
- CCHL1A2
- CNTN2
- COL29A1
- COL4A1
- COL4A2
- COL4A3
- COL4A4
- COL4A5
- COL6A1
- COL6A2
- COL6A3
- COL6A5
- COL6A6
- COL9A1
- COL9A2
- COL9A3
- CSPG3
- EVN
- GDNF
- GDNFRA
- GDNFRB
- GFRA1
- GFRA2
- GFRA4
- KIAA1120
- KIAA1123
- MYSB
- NCAM
- NCAM1
- NCAN
- NEUR
- NRTN
- PRIP
- PRNP
- PRP
- PSPN
- PST
- PST1
- RETL1
- RETL2
- SIAT8B
- SIAT8D
- ST8SIA2
- ST8SIA4
- STX
- TAG1
- TAX1
- TRNR1
- TRNR2
- VWA4
|
Homo sapiens (human)
|
|
Defective GALNT12 causes CRCS1
|
|
|
- C6orf205
- CA125
- DRCC1
- GALNT12
- KIAA1359
- MG2
- MUC1
- MUC11
- MUC12
- MUC13
- MUC15
- MUC16
- MUC17
- MUC19
- MUC2
- MUC20
- MUC21
- MUC3
- MUC3A
- MUC3B
- MUC4
- MUC5
- MUC5AC
- MUC5B
- MUC6
- MUC7
- MUCL1
- PUM
- RECC
- SBEM
- SMUC
|
Homo sapiens (human)
|
|
Beta-ketothiolase deficiency
|
|
|
|
Homo sapiens (human)
|
|
Regulation of IFNG signaling
|
|
|
- CIS3
- DDXBP1
- HCP
- IFNG
- IFNGR1
- IFNGR2
- IFNGT1
- JAK1
- JAK1A
- JAK1B
- JAK2
- PIAS1
- PTP1B
- PTP1C
- PTP2C
- PTPN1
- PTPN11
- PTPN6
- SHPTP2
- SMT3C
- SMT3H3
- SOCS1
- SOCS3
- SSI1
- SSI3
- SUMO1
- TIP3
- UBL1
|
Homo sapiens (human)
|
|
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha)
|
|
|
- COCA2
- EXO1
- EXOI
- GTBP
- HEX1
- KIAA0039
- LIG1
- MLH1
- MSH2
- MSH6
- PCNA
- PMS2
- PMSL2
- POLD
- POLD1
- POLD2
- POLD3
- POLD4
- POLDS
- REPA1
- REPA2
- REPA3
- RPA1
- RPA14
- RPA2
- RPA3
- RPA32
- RPA34
- RPA70
|
Homo sapiens (human)
|
|
Astrocytic Glutamate-Glutamine Uptake And Metabolism
|
|
|
- ATA1
- EAAT1
- EAAT2
- GLAST
- GLAST1
- GLNS
- GLT1
- GLUL
- NAT2
- SAT1
- SLC1A2
- SLC1A3
- SLC38A1
- SNAT1
|
Homo sapiens (human)
|
|
Inhibition of replication initiation of damaged DNA by RB1/E2F1
|
|
|
- DP1
- DP2
- E2F1
- POLA
- POLA1
- POLA2
- PPP2CA
- PPP2CB
- PPP2R1A
- PPP2R1B
- PPP2R3B
- PPP2R3L
- PRIM1
- PRIM2
- PRIM2A
- RB1
- RBBP3
- TFDP1
- TFDP2
|
Homo sapiens (human)
|
|
Defective MAOA causes BRUNS
|
|
|
|
Homo sapiens (human)
|
|
Defective RIPK1-mediated regulated necrosis
|
|
|
- CASP8
- FADD
- MCH5
- MORT1
- RIP
- RIP1
- RIPK1
- TRADD
- TRAF2
- TRAP3
|
Homo sapiens (human)
|
|
LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production
|
|
|
- CBP
- CREBBP
- CTNNB
- CTNNB1
- EP300
- GCF2
- IRF3
- LRRFIP1
- P300
- TRIP
|
Homo sapiens (human)
|
|
Defective SLC17A8 causes autosomal dominant deafness 25 (DFNA25)
|
|
|
|
Homo sapiens (human)
|
|
Beta oxidation of lauroyl-CoA to decanoyl-CoA-CoA
|
|
|
- ACADL
- ECHS1
- HAD
- HAD1
- HADH
- HADHA
- HADHB
- HADHSC
- SCHAD
|
Homo sapiens (human)
|
|