Gene
|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
2833 |
Gene nameGene Name - the full gene name approved by the HGNC.
|
C-X-C motif chemokine receptor 3 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
|
CXCR3 |
SynonymsGene synonyms aliases
|
CD182, CD183, CKR-L2, CMKAR3, GPR9, IP10-R, Mig-R, MigR |
ChromosomeChromosome number
|
X |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
Xq13.1 |
SummarySummary of gene provided in NCBI Entrez Gene.
|
This gene encodes a G protein-coupled receptor with selectivity for three chemokines, termed CXCL9/Mig (monokine induced by interferon-g), CXCL10/IP10 (interferon-g-inducible 10 kDa protein) and CXCL11/I-TAC (interferon-inducible T cell a-chemoattractant) |
miRNAmiRNA information provided by mirtarbase database.
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Transcription factors
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
|
UniProt ID |
P49682 |
Protein name |
C-X-C chemokine receptor type 3 (CXC-R3) (CXCR-3) (CKR-L2) (G protein-coupled receptor 9) (Interferon-inducible protein 10 receptor) (IP-10 receptor) (CD antigen CD183) |
Protein function |
[Isoform 1]: Receptor for the C-X-C chemokine CXCL9, CXCL10 and CXCL11 and mediates the proliferation, survival and angiogenic activity of human mesangial cells (HMC) through a heterotrimeric G-protein signaling pathway (PubMed:12782716). Binds |
PDB |
8HNK
,
8HNL
,
8HNM
,
8HNN
,
8K2W
,
8K2X
,
8XXY
,
8XXZ
,
8XYI
,
8XYK
,
8Y0H
,
8Y0N
|
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00001 |
7tm_1 |
70 → 318 |
7 transmembrane receptor (rhodopsin family) |
Family |
|
Sequence |
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Sequence length |
368 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
|
Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Autoimmune diseases |
Autoimmune Diseases |
rs41285370, rs869025224 |
12517959 |
Dermatitis |
Dermatitis, Atopic, Contact Dermatitis |
rs61816761, rs150597413, rs138726443, rs201356558, rs149484917, rs372754256, rs747301529, rs567795279, rs745915174 |
18249437, 25724174 |
Glomerulonephritis |
Glomerulonephritis |
rs778043831 |
12517959 |
|
Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Alopecia areata |
Alopecia Areata |
|
22358057 |
Bright disease |
Bright Disease |
|
12517959 |
Eczema |
Eczema, Infantile |
|
18249437 |
Pleural diseases |
Pleural Diseases |
|
21357438 |
Stroke |
Cerebrovascular accident, Acute Cerebrovascular Accidents |
|
12374626 |
|