Description |
solute carrier family 18 member A1 |
membrane spanning 4-domains A13 |
Image |
No pdb structure |
No pdb structure |
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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- Congenital heart disease (maternal effect) ( 28468790)
- Major depressive disorder ( 29317602)
- Metabolite levels (X-11787) ( 23934736)
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Interacting Genes |
61 interacting genes:
AGTRAP
ANKRD46
APOL2
BRICD5
C2CD2L
CCL4
CCL4L2
CNIH1
COL4A5
CTSA
CXCL16
CYB561D2
FAM3C
FCER1G
FXYD3
GIMAP1
GJB2
GPR151
LAT
MALL
MFSD6
MGAM
MIP
MS4A1
MS4A13
NEU1
NRM
OLFM4
ORMDL1
PEX16
PLP1
PLP2
PMP22
PNLIPRP1
PPP3CC
RPRM
SLC30A2
SLC30A8
SLC35B4
SLC35G1
SLC38A7
SLC39A2
SMCO4
SMIM1
STX2
STX8
TFRC
TMEM120B
TMEM128
TMEM14A
TMEM14B
TMEM203
TMEM218
TMEM239
TMEM42
TMEM60
TMEM65
TMEM86A
VAMP5
YIPF4
YIPF6
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61 interacting genes:
AQP2
AQP6
ASGR2
ATP6V0E1
BEST1
BIK
CBARP
CD79A
CLDN7
CREB3L1
CREB3L3
DAGLA
EBP
EDA
EREG
ERGIC3
EVA1A
FAM209A
FAM210B
FFAR2
GJA4
GJA5
GJA8
GJB1
GJB5
GJB6
GJC3
GPR152
HERPUD2
JSRP1
KCNMB4
KLRC1
LHFPL5
LRRC3B
MMGT1
MS4A3
NPDC1
ODF4
POMK
RAMP1
RHCG
RNF185
SCN3B
SLC12A7
SLC13A4
SLC16A2
SLC18A1
SLC30A2
SLC39A2
SLC7A1
SPAG4
SSMEM1
TBXA2R
TLCD4
TM4SF18
TMC4
TMEM14B
TMEM237
TMEM52B
TMEM74
VSIR
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Entrez ID |
6570 |
503497 |
HPRD ID |
01897 |
17604 |
Ensembl ID |
ENSG00000036565
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ENSG00000204979
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Uniprot IDs |
P54219
Q96GL6
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Q5J8X5
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PDB IDs |
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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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