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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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133396
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Interleukin 31 receptor A |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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IL31RA |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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CRL, CRL3, GLM-R, GLMR, GPL, IL-31RA, PLCA2, PRO21384, hGLM-R, zcytoR17 |
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Chromosome
Chromosome number
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5 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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5q11.2 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene belongs to the type I cytokine receptor family. This receptor, with homology to gp130, is expressed on monocytes, and is involved in IL-31 signaling via activation of STAT-3 and STAT-5. It functions either as a monomer, or |
| UniProt ID |
Q8NI17
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| Protein name |
Interleukin-31 receptor subunit alpha (IL-31 receptor subunit alpha) (IL-31R subunit alpha) (IL-31R-alpha) (IL-31RA) (Cytokine receptor-like 3) (GLM-R) (hGLM-R) (Gp130-like monocyte receptor) (Gp130-like receptor) (ZcytoR17) |
| Protein function |
Associates with OSMR to form the interleukin-31 receptor which activates STAT3 and to a lower extent STAT1 and STAT5 (PubMed:11877449, PubMed:14504285, PubMed:15194700, PubMed:15627637). May function in skin immunity (PubMed:15184896). Mediates |
| Family and domains |
Pfam
| Accession |
ID |
Position in sequence |
Description |
Type |
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PF09240
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IL6Ra-bind |
27 → 119 |
Interleukin-6 receptor alpha chain, binding |
Domain |
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PF00041
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fn3 |
123 → 215 |
Fibronectin type III domain |
Domain |
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PF00041
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fn3 |
425 → 507 |
Fibronectin type III domain |
Domain |
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| Tissue specificity |
TISSUE SPECIFICITY: Expressed in CD14- and CD56-positive blood cells (PubMed:11877449). Expressed in macrophages (PubMed:16461143, PubMed:18439099). Expressed in keratinocytes (PubMed:21261663). Expressed in a subset of dorsal root ganglia neurons (at pro |
| Sequence |
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| Sequence length |
732 |
| Interactions |
View interactions
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Causal
Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
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| Disease merge term |
Disease name |
dbSNP ID |
References |
| Amyloidosis |
amyloidosis, primary localized cutaneous, 2 |
rs1561123748 |
N/A |
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Unknown
Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
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| Disease merge term |
Disease name |
Evidence |
References |
Source |
| Localized Cutaneous Amyloidosis |
familial primary localized cutaneous amyloidosis |
N/A |
N/A |
GenCC |
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