Gene Gene information from NCBI Gene database.
Entrez ID 133396
Gene name Interleukin 31 receptor A
Gene symbol IL31RA
Synonyms (NCBI Gene)
CRLCRL3GLM-RGLMRGPLIL-31RAPLCA2PRO21384hGLM-RzcytoR17
Chromosome 5
Chromosome location 5q11.2
Summary 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
SNPs SNP information provided by dbSNP.
1
SNP ID Visualize variation Clinical significance Consequence
rs1561123748 C>T Pathogenic Coding sequence variant, missense variant, genic downstream transcript variant
miRNA miRNA information provided by mirtarbase database.
7
miRTarBase ID miRNA Experiments Reference
MIRT019063 hsa-miR-335-5p Microarray 18185580
MIRT1550119 hsa-miR-4660 CLIP-seq
MIRT1550120 hsa-miR-885-3p CLIP-seq
MIRT1550119 hsa-miR-4660 CLIP-seq
MIRT1550120 hsa-miR-885-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
39
GO ID Ontology Definition Evidence Reference
GO:0000165 Process MAPK cascade NAS 11877449
GO:0002067 Process Glandular epithelial cell differentiation IEA
GO:0002376 Process Immune system process IEA
GO:0002438 Process Acute inflammatory response to antigenic stimulus IEA
GO:0003713 Function Transcription coactivator activity NAS 11877449
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
609510 18969 ENSG00000164509
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8NI17
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
PF09240 IL6Ra-bind 27 119 Interleukin-6 receptor alpha chain, binding Domain
PF00041 fn3 123 215 Fibronectin type III domain Domain
PF00041 fn3 425 507 Fibronectin type III domain Domain
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
MMWTWALWMLPSLCKFSLAALPAKPENISCVYYYRKNLTCTWSPGKETSYTQYTVKRTYA
FGEKHDNCTTNSSTSENRASCSFFLPRITIPDNYTIEVEAENGDGVIKSHMTYWRLENI
A
KTEPPKIFRVKPVLGIKRMIQIEWIKPELAPVSSDLKYTLRFRTVNSTSWMEVNFAKNRK
DKNQTYNLTGLQPFTEYVIALRCAVKESKFWSDWS
QEKMGMTEEEAPCGLELWRVLKPAE
ADGRRPVRLLWKKARGAPVLEKTLGYNIWYYPESNTNLTETMNTTNQQLELHLGGESFWV
SMISYNSLGKSPVATLRIPAIQEKSFQCIEVMQACVAEDQLVVKWQSSALDVNTWMIEWF
PDVDSEPTTLSWESVSQATNWTIQQDKLKPFWCYNISVYPMLHDKVGEPYSIQAYAKEGV
PSEGPETKVENIGVKTVTITWKEIPKSERKGIICNYTIFYQAEGGKGFSKTVNSSILQYG
LESLKRKTSYIVQVMASTSAGGTNGTS
INFKTLSFSVFEIILITSLIGGGLLILIILTVA
YGLKKPNKLTHLCWPTVPNPAESSIATWHGDDFKDKLNLKESDDSVNTEDRILKPCSTPS
DKLVIDKLVVNFGNVLQEIFTDEARTGQENNLGGEKNGYVTCPFRPDCPLGKSFEELPVS
PEIPPRKSQYLRSRMPEGTRPEAKEQLLFSGQSLVPDHLCEEGAPNPYLKNSVTAREFLV
SEKLPEHTKGEV
Sequence length 732
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Cytokine-cytokine receptor interaction
JAK-STAT signaling pathway
  IL-6-type cytokine receptor ligand interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
27
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Amyloidosis, primary localized cutaneous, 2 Pathogenic rs1561123748 RCV000023775
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cervical cancer Benign rs148721785 RCV005935394
Familial pancreatic carcinoma Benign rs148721785 RCV005935395
IL31RA-related disorder Benign; Likely benign; Conflicting classifications of pathogenicity rs9632389, rs17701253, rs74629680, rs544735425, rs371900126, rs148721785, rs161704, rs59086632, rs183184063, rs144829917, rs73118479 RCV003973266
RCV003914191
RCV003911868
RCV003944028
RCV003939626
RCV003979188
RCV003982157
RCV003976676
RCV003966817
RCV003950738
RCV003916224
Malignant lymphoma, large B-cell, diffuse Benign rs16884641, rs148721785 RCV005920620
RCV005935396
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Amyloidosis Primary Cutaneous Associate 19690585
Asthma Associate 26956917, 35606283
Carcinoma Hepatocellular Associate 36685508
Death Associate 39523440
Dermatomyositis Associate 29494763
Endometrial Neoplasms Associate 38108937
Inflammation Associate 22041865
Lymphoma T Cell Cutaneous Associate 27001482
Neoplasms Associate 27906189, 36359832, 39523440
Neuroblastoma Associate 21436895, 23222812