CCR3 (C-C motif chemokine receptor 3)
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Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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1232 |
Gene nameGene Name - the full gene name approved by the HGNC.
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C-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.
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CCR3 |
SynonymsGene synonyms aliases
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C C CKR3, CC-CKR-3, CD193, CKR 3, CKR3, CMKBR3 |
ChromosomeChromosome number
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3 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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3p21.31 |
SummarySummary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene is a receptor for C-C type chemokines. It belongs to family 1 of the G protein-coupled receptors. This receptor binds and responds to a variety of chemokines, including eotaxin (CCL11), eotaxin-3 (CCL26), MCP-3 (CCL7), MCP-4 (CCL13), and RANTES (CCL5). It is highly expressed in eosinophils and basophils, and is also detected in TH1 and TH2 cells, as well as in airway epithelial cells. This receptor may contribute to the accumulation and activation of eosinophils and other inflammatory cells in the allergic airway. It is also known to be an entry co-receptor for HIV-1. This gene and seven other chemokine receptor genes form a chemokine receptor gene cluster on the chromosomal region 3p21. Alternatively spliced transcript variants have been described. [provided by RefSeq, Sep 2009] |
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
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UniProt ID |
P51677 |
Protein name |
C-C chemokine receptor type 3 (C C CKR3) (C-C CKR-3) (CC-CKR-3) (CCR-3) (CCR3) (CKR 3) (CKR3) (Eosinophil eotaxin receptor) (CD antigen CD193) |
Protein function |
Receptor for C-C type chemokine. Binds and responds to a variety of chemokines, including CCL11, CCL26, CCL7, CCL13, RANTES(CCL5) and CCL15 (PubMed:7622448, PubMed:8642344, PubMed:8676064). Subsequently transduces a signal by increasing the intracellular calcium ions level (PubMed:8676064). In addition acts as a possible functional receptor for NARS1 (PubMed:30171954). ; (Microbial infection) Alternative coreceptor with CD4 for HIV-1 infection. |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00001 |
7tm_1 |
51 → 301 |
7 transmembrane receptor (rhodopsin family) |
Family |
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Sequence |
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Sequence length |
355 |
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
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Autoimmune diseases |
Autoimmune Diseases |
rs41285370, rs869025224 |
21383967 |
Asthma |
Asthma, Asthma, Aspirin-Induced |
rs324981, rs121912630, rs150116809, rs4950928, rs708494, rs1581842283 |
21150878, 20485159 |
Rheumatoid arthritis |
Rheumatoid Arthritis, Rheumatoid Arthritis, Systemic Juvenile |
rs3766379, rs3792876, rs2071592, rs3087456, rs587776843, rs1566328963 |
26546613, 23603761 |
Pulmonary fibrosis |
Pulmonary Fibrosis |
rs121918666, rs199422300, rs121917737, rs121917834, rs199422294, rs201159197, rs199422297, rs199422305, rs751381953, rs876661305, rs878853260, rs863223336, rs786205702, rs1555811762, rs1060502990, rs1555903332, rs1554038539, rs1554042899, rs938938578 |
16314464 |
Multiple sclerosis |
Multiple Sclerosis |
rs104895219, rs-1, rs483353022, rs483353023, rs483353028, rs483353029, rs483353024, rs483353030, rs3207617, rs483353031, rs483353032, rs483353033, rs483353034, rs483353035, rs483353036, rs483353039, rs483353038, rs61731956, rs568165874, rs767480544 |
22190364 |
Dermatitis |
Dermatitis, Atopic |
rs61816761, rs150597413, rs138726443, rs201356558, rs149484917, rs372754256, rs747301529, rs567795279, rs745915174 |
18249437 |
Arthritis |
Systemic onset juvenile chronic arthritis |
rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470 |
23603761 |
Behcet syndrome |
Behcet Syndrome |
rs886040969, rs886039866, rs746055479, rs752615209, rs774164456, rs751454741 |
23291587 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Celiac disease |
Celiac Disease |
rs2305764, rs35218876 |
22057235, 20190752, 26546613, 24999842 |
Alveolitis |
Alveolitis, Fibrosing |
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16314464 |
Eczema |
Eczema, Infantile |
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18249437 |
Grand mal status epilepticus |
Grand Mal Status Epilepticus |
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19490431 |
Immune system diseases |
Immune System Diseases |
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21383967 |
Nonconvulsive status epilepticus |
Non-Convulsive Status Epilepticus |
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19490431 |
Oligoarticular arthritis |
Oligoarticular Juvenile Idiopathic Arthritis |
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23603761 |
Pauciarticular chronic arthritis |
Juvenile pauciarticular chronic arthritis |
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23603761 |
Petit mal status |
Petit mal status |
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19490431 |
Seronegative polyarthritis |
Polyarticular Juvenile Idiopathic Arthritis, Rheumatoid Factor Negative |
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23603761 |
Status epilepticus |
Status Epilepticus, Complex Partial Status Epilepticus, Status Epilepticus, Subclinical |
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19490431 |
Still disease |
Juvenile-Onset Still Disease |
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23603761 |
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