| Name |
ATPase H+ transporting V0 subunit b |
solute carrier family 10 member 1 |
| Structure |
|
|
| GO Annotations |
Cellular Component |
|
|
| Molecular Function |
|
|
| Biological Process |
|
|
| Pathways |
|
|
| Drugs |
|
|
| GWAS |
- Autism spectrum disorder or schizophrenia ( 28540026
)
|
|
| Interacting Genes |
28 interacting genes:
ADGRG3
ADRB2
APOD
COL4A5
EMP1
FAM210B
FAS
GJA8
GPR42
GPR61
INSIG2
IRAK3
KLRC1
MFF
MIP
MS4A3
MTNR1B
NRM
SLC10A1
SLC2A5
SNTA1
SPACA1
STOM
TM4SF19
TMEM242
VMA21
YWHAE
YWHAG
|
115 interacting genes:
ABHD16A
ACSL5
AGPAT3
APOL3
ARL6IP6
ASGR1
ATP13A1
ATP6V0B
BMP10
BTN2A2
C2
C3orf52
C8A
CDIPT
CFHR5
CFTR
CLDN19
CMTM3
COX20
CXCL9
CYB5B
CYB5R3
DERL1
DGAT2L6
EMC6
EMD
FA2H
FAM241B
FAXDC2
FCER1G
FDFT1
FKBP8
FXYD3
FXYD6
FXYD6-FXYD2
GAST
GDE1
GIMAP5
GOSR2
GPR151
GPR152
IFITM2
IFITM3
IFTAP
INSIG2
LNPEP
LRP10
LSS
MAL
MALL
MFSD6
MS4A1
MYADML2
NEU1
NINJ2
NKG7
ORMDL1
ORMDL2
ORMDL3
OTOP3
PEDS1-UBE2V1
PEX16
PKMYT1
PMP22
RABAC1
RTP2
RUSF1
SACM1L
SCAMP4
SEC22A
SELENOK
SERP1
SFT2D1
SFT2D2
SFXN1
SLC12A7
SLC16A13
SLC25A46
SLC29A2
SLC35E4
SLC38A1
SLC38A7
SLC41A1
SLC66A2
SLC7A3
SMPD2
STATH
STX12
STX7
TAP1
TFRC
TMBIM1
TMEM119
TMEM120B
TMEM121
TMEM147
TMEM222
TMEM234
TMEM239
TMEM242
TMEM60
TMEM97
TMUB2
TOMM6
TRARG1
TSPO2
TVP23B
UBIAD1
UNC50
UPK1B
VAMP3
VAPB
YIF1A
YIPF4
YIPF6
|
| Entrez ID |
533 |
6554 |
| HPRD ID |
04759
|
01672
|
| Ensembl ID |
ENSG00000117410
|
ENSG00000100652
|
| Uniprot IDs |
E9PNL3
Q99437
|
B2RA41
Q14973
|
| PDB IDs |
6WLW
6WM2
6WM3
6WM4
7U4T
7UNF
|
7FCI
7PQG
7PQQ
7VAD
7VAG
7WSI
7ZYI
8HRX
8HRY
8RQF
|
| GO Terms Enriched among Interactors |
|
|