IL10RA (interleukin 10 receptor subunit alpha)
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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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3587 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Interleukin 10 receptor subunit alpha |
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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IL10RA |
SynonymsGene synonyms aliases
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CD210, CD210a, CDW210A, HIL-10R, IL-10R1, IL10R |
ChromosomeChromosome number
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11 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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11q23.3 |
SummarySummary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene is a receptor for interleukin 10. This protein is structurally related to interferon receptors. It has been shown to mediate the immunosuppressive signal of interleukin 10, and thus inhibits the synthesis of proinflammator |
SNPsSNP information provided by dbSNP.
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SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs137853579 |
G>A,C |
Pathogenic |
Coding sequence variant, non coding transcript variant, 5 prime UTR variant, missense variant |
rs137853580 |
C>T |
Pathogenic |
Coding sequence variant, non coding transcript variant, intron variant, missense variant |
rs138929400 |
T>G |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, non coding transcript variant, missense variant |
rs148808529 |
T>C |
Uncertain-significance, conflicting-interpretations-of-pathogenicity |
Non coding transcript variant, synonymous variant, coding sequence variant |
rs149491038 |
C>T |
Pathogenic |
Non coding transcript variant, missense variant, coding sequence variant |
rs199604463 |
G>A |
Conflicting-interpretations-of-pathogenicity |
Non coding transcript variant, coding sequence variant, synonymous variant |
rs201396764 |
C>T |
Uncertain-significance, conflicting-interpretations-of-pathogenicity |
Non coding transcript variant, coding sequence variant, missense variant |
rs201643277 |
A>G |
Uncertain-significance, conflicting-interpretations-of-pathogenicity |
Non coding transcript variant, coding sequence variant, 5 prime UTR variant, missense variant |
rs368287711 |
C>A,T |
Pathogenic |
Missense variant, non coding transcript variant, coding sequence variant, synonymous variant, intron variant |
rs377525753 |
G>A |
Uncertain-significance, conflicting-interpretations-of-pathogenicity |
5 prime UTR variant, synonymous variant, coding sequence variant, non coding transcript variant |
rs560128585 |
A>C |
Conflicting-interpretations-of-pathogenicity, uncertain-significance |
5 prime UTR variant, synonymous variant, coding sequence variant, non coding transcript variant |
rs1192830343 |
C>T |
Likely-pathogenic |
Stop gained, non coding transcript variant, coding sequence variant |
rs1419560997 |
G>A |
Pathogenic |
Synonymous variant, coding sequence variant, non coding transcript variant |
rs1591263883 |
C>T |
Pathogenic |
Coding sequence variant, stop gained, non coding transcript variant |
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miRNAmiRNA information provided by mirtarbase database.
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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 |
Q13651 |
Protein name |
Interleukin-10 receptor subunit alpha (IL-10 receptor subunit alpha) (IL-10R subunit alpha) (IL-10RA) (CDw210a) (Interleukin-10 receptor subunit 1) (IL-10R subunit 1) (IL-10R1) (CD antigen CD210) |
Protein function |
Cell surface receptor for the cytokine IL10 that participates in IL10-mediated anti-inflammatory functions, limiting excessive tissue disruption caused by inflammation. Upon binding to IL10, induces a conformational change in IL10RB, allowing IL |
PDB |
1J7V
,
1LQS
,
1Y6K
,
1Y6M
,
1Y6N
,
5IXI
,
6X93
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Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF01108 |
Tissue_fac |
4 → 111 |
Tissue factor |
Family |
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Sequence |
MLPCLVVLLAALLSLRLGSDAHGTELPSPPSVWFEAEFFHHILHWTPIPNQSESTCYEVA LLRYGIESWNSISNCSQTLSYDLTAVTLDLYHSNGYRARVRAVDGSRHSNWTVTNTRFSV DEVTLTVGSVNLEIHNGFILGKIQLPRPKMAPANDTYESIFSHFREYEIAIRKVPGNFTF THKKVKHENFSLLTSGEVGEFCVQVKPSVASRSNKGMWSKEECISLTRQYFTVTNVIIFF AFVLLLSGALAYCLALQLYVRRRKKLPSVLLFKKPSPFIFISQRPSPETQDTIHPLDEEA FLKVSPELKNLDLHGSTDSGFGSTKPSLQTEEPQFLLPDPHPQADRTLGNREPPVLGDSC SSGSSNSTDSGICLQEPSLSPSTGPTWEQQVGSNSRGQDDSGIDLVQNSEGRAGDTQGGS ALGHHSPPEPEVPGEEDPAAVAFQGYLRQTRCAEEKATKTGCLEEESPLTDGLGPKFGRC LVDEAGLHPPALAKGYLKQDPLEMTLASSGAPTGQWNQPTEEWSLLALSSCSDLGISDWS FAHDLAPLGCVAAPGGLLGSFNSDLVTLPLISSLQSSE
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Sequence length |
578 |
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 |
Inflammatory bowel disease |
Inflammatory Bowel Diseases, INFLAMMATORY BOWEL DISEASE 28, AUTOSOMAL RECESSIVE |
rs137853579, rs137853580, rs121909601, rs149491038, rs368287711, rs387907326, rs587777338, rs758439420, rs139868987, rs750447828, rs368138379, rs1329427406, rs1264862631, rs1192830343, rs1373354533, rs1419560997, rs1591263883, rs1989014468 |
27302973, 29059189, 24785691, 23839161, 27302973, 19890111 |
Schizophrenia |
Schizophrenia |
rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 |
17066477 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Enterocolitis |
Enterocolitis |
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Folliculitis |
Folliculitis |
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Perianal abscess |
Perianal abscess |
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Pyoderma |
Pyoderma |
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Ulcerative colitis |
Ulcerative Colitis |
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27302973 |
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