Description |
membrane spanning 4-domains A13 |
solute carrier family 7 member 1 |
Image |
No pdb structure |
No pdb structure |
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 |
- Congenital heart disease (maternal effect) ( 28468790)
- Major depressive disorder ( 29317602)
- Metabolite levels (X-11787) ( 23934736)
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Interacting Genes |
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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57 interacting genes:
ADGRB3
APOA2
APP
AQP6
ATP6V0C
C8A
CBLIF
CCL4
CCL4L2
CD40
CD79A
CDIPT
CERS4
CMTM2
COMT
CREB3L1
EMC6
FAM241B
FATE1
FCER1G
GALNT15
GET1
GLB1
GPR152
HERPUD2
LEPROT
LEPROTL1
LMNA
MFF
MGST3
MS4A13
NUCB2
ORMDL3
PDCD1LG2
PNLIPRP1
PSCA
PTPN9
RNF144A
SACM1L
SCN3B
SEC23A
SLC10A6
SLC18A2
SLC30A2
SLC39A2
SLC39A9
SLC52A1
SMCO4
ST6GAL2
STIM1
TMBIM6
TMEM14A
TMEM19
TMEM237
TRARG1
TSPO2
YIPF4
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Entrez ID |
503497 |
6541 |
HPRD ID |
17604 |
00091 |
Ensembl ID |
ENSG00000204979
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ENSG00000139514
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Uniprot IDs |
Q5J8X5
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A0A024RDQ9
P30825
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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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