Description |
claudin 7 |
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 |
77 interacting genes:
AIG1
ANKRD46
APOD
AQP2
ASGR1
BCL2L2
BET1
BMP10
C3orf52
CD53
CD72
CLN6
CMTM5
CNIH1
COL4A5
CXCL16
CXCL9
CYB561A3
CYB561D2
CYB5B
CYBC1
EDDM3B
EMP3
EPCAM
ERG28
ERMP1
FAXDC2
FXYD6
GIMAP5
GLP1R
GPR37L1
HGD
IGFBP5
ITM2A
JAGN1
LAT
LEPROTL1
LPAR3
LSMEM2
MAL
MALL
MFSD5
MS4A13
NDUFB11
NIPAL4
NKG7
OLFM4
PGAP2
PLN
RHOXF2
RPRM
RTP2
SCAMP4
SCARF1
SEC22B
SERTM1
SLC38A7
SYNE4
TJP1
TMEM100
TMEM11
TMEM128
TMEM140
TMEM147
TMEM44
TMEM60
TMEM97
TNF
TRARG1
TSPAN33
UBIAD1
UNC93B1
UPK1B
UPK2
VAMP3
VAMP5
VSTM1
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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 |
1366 |
503497 |
HPRD ID |
07633 |
17604 |
Ensembl ID |
ENSG00000181885
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ENSG00000204979
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Uniprot IDs |
A0A384ME58
F5H496
O95471
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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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