Description |
solute carrier family 7 member 14 |
ninjurin 2 |
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 |
- Obesity (extreme) ( 30677029)
- Spontaneous preterm birth without premature rupture of membranes ( 31194736)
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Interacting Genes |
47 interacting genes:
ACSL5
ADGRE2
AGTRAP
AIG1
APOL3
BET1
BNIP1
BNIP2
C1GALT1
CBLIF
CCDC167
CCL4L2
CD53
CMTM5
DCBLD2
DERL1
EOGT
ERMP1
FAM209A
FAM20B
FATE1
FCER1G
FKBP7
IL10RA
LINC00839
LTC4S
MFF
MGLL
MMGT1
NINJ2
NSG1
PLPP6
PRB1
SCARF1
SCD
SMCO4
TECR
TMEM128
TMEM31
TRARG1
TREX1
UBIAD1
VAMP2
VKORC1
YIPF4
YIPF6
ZFPL1
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74 interacting genes:
AMIGO1
AQP6
ARL13B
BCL2L13
BTNL9
CD69
CD79A
CEACAM3
CHODL
CLEC17A
CLEC7A
CPLX4
CREB3L1
CYBC1
EBP
ELOVL4
ELOVL5
EREG
ERGIC3
ERVFRD-1
EVI2B
FAM209A
FAM210B
FCGRT
FCRL4
FNDC9
GJA1
GPR152
GPR42
ICAM3
IFNGR1
IL3RA
JAGN1
KCNJ6
KIR2DL3
KIR3DL3
LDLRAD1
LHFPL5
LMNA
LYPD5
LYVE1
M6PR
MGST3
MMGT1
MR1
MUC1
ODF4
PIGP
PVR
RIC3
RNASEK
SCN3B
SLAMF8
SLC10A1
SLC10A6
SLC66A1
SLC7A14
SLC7A8
STX1A
STX2
TM4SF20
TMEM101
TMEM139
TMEM14B
TMEM31
TMEM51
TMEM52B
TMEM86B
TMEM9
TMPRSS2
TMX2
TSPAN12
VMA21
VSIG1
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Entrez ID |
57709 |
4815 |
HPRD ID |
17222 |
09530 |
Ensembl ID |
ENSG00000013293
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ENSG00000171840
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Uniprot IDs |
Q8TBB6
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A0A590UJR9
B4DJC1
F5H3L1
F8WBZ3
Q9NZG7
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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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