Description |
solute carrier family 10 member 1 |
ATPase H+ transporting V0 subunit b |
Image |
No pdb structure |
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GO Annotations |
Cellular Component |
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Molecular Function |
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Biological Process |
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Pathways |
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Drugs |
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Diseases |
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GWAS |
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- Autism spectrum disorder or schizophrenia ( 28540026)
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Interacting Genes |
91 interacting genes:
ABHD16A
ACSL5
AGPAT3
ARL6IP6
ASGR1
ATP6V0B
BMP10
C2
C8A
CFHR5
CLDN19
CMTM3
COX20
CXCL9
CYB5R3
DERL1
DGAT2L6
FA2H
FAM241B
FAXDC2
FCER1G
FDFT1
FXYD3
FXYD6
FXYD6-FXYD2
GAST
GDE1
GIMAP5
GOSR2
GPR151
GPR152
IFITM2
IFITM3
IFTAP
LRP10
LSS
MAL
MALL
MFSD6
MS4A1
MYADML2
NEU1
NINJ2
ORMDL1
ORMDL2
ORMDL3
OTOP3
PEDS1-UBE2V1
PEX16
PKMYT1
RUSF1
SACM1L
SCAMP4
SELENOK
SFT2D1
SFT2D2
SFXN1
SLC12A7
SLC16A13
SLC25A46
SLC29A2
SLC35E4
SLC38A1
SLC38A7
SLC41A1
SLC66A2
SLC7A3
SMPD2
STX7
TAP1
TFRC
TMBIM1
TMEM119
TMEM120B
TMEM121
TMEM147
TMEM222
TMEM234
TMEM239
TMEM242
TMEM60
TMUB2
TOMM6
TRARG1
TSPO2
TVP23B
UNC50
VAMP3
YIF1A
YIPF4
YIPF6
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34 interacting genes:
ADGRG3
ADRB2
APOD
BPI
CCL19
COL4A5
DAPK2
EMP1
FAM210B
FAS
GJA8
GPR42
GPR61
INSIG2
IRAK3
KLRC1
MFF
MIP
MS4A3
MTNR1B
NRM
RPS26P15
SLC10A1
SLC2A5
SNTA1
SPACA1
STOM
TM4SF19
TMEM242
TTC39A
VMA21
YWHAE
YWHAG
ZFYVE9
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Entrez ID |
6554 |
533 |
HPRD ID |
01672 |
04759 |
Ensembl ID |
ENSG00000100652
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ENSG00000117410
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Uniprot IDs |
B2RA41
Q14973
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E9PNL3
Q99437
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PDB IDs |
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6WLW
6WM2
6WM3
6WM4
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
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Tagcloud (Difference) ? |
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Tagcloud (Intersection) ? |
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