Description |
solute carrier family 39 member 2 |
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 |
54 interacting genes:
AQP1
AQP6
ARL13B
BCL2L2
BTN2A2
C3orf52
C4orf3
CD79A
CLCA4
CNR2
COL4A5
COMT
CREB3L1
CXCR2
CYB561
EHHADH
EMC6
FCER1G
FXYD3
FXYD6
GJA8
GPR152
GPR42
IL6R
KCNAB1
KCNAB2
KCNJ15
LY6G6C
MFSD6
MS4A13
PLN
PNLIPRP1
POR
SEC22A
SLC18A1
SLC30A2
SLC30A8
SLC39A1
SLC39A9
SLC66A1
SLC7A1
SSMEM1
ST6GAL2
STATH
TMEM107
TMEM14B
TMEM229B
TMEM237
TMEM54
TMEM60
TMEM86A
TRHR
UPK1B
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 |
29986 |
503497 |
HPRD ID |
15385 |
17604 |
Ensembl ID |
ENSG00000165794
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ENSG00000204979
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Uniprot IDs |
Q9NP94
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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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