Gene Gene information from NCBI Gene database.
Entrez ID 84818
Gene name Interleukin 17 receptor C
Gene symbol IL17RC
Synonyms (NCBI Gene)
CANDF9IL17-RLIL17RL
Chromosome 3
Chromosome location 3p25.3|3p25.3-p24.1
Summary This gene encodes a single-pass type I membrane protein that shares similarity with the interleukin-17 receptor (IL-17RA). Unlike IL-17RA, which is predominantly expressed in hemopoietic cells, and binds with high affinity to only IL-17A, this protein is
SNPs SNP information provided by dbSNP.
3
SNP ID Visualize variation Clinical significance Consequence
rs559955121 C>T Likely-pathogenic Coding sequence variant, stop gained, non coding transcript variant
rs773852926 C>T Pathogenic Non coding transcript variant, coding sequence variant, stop gained
rs1057518751 C>T Pathogenic Stop gained, non coding transcript variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
5
miRTarBase ID miRNA Experiments Reference
MIRT028962 hsa-miR-26b-5p Microarray 19088304
MIRT052327 hsa-let-7b-5p CLASH 23622248
MIRT050548 hsa-miR-20a-5p CLASH 23622248
MIRT036625 hsa-miR-940 CLASH 23622248
MIRT036625 hsa-miR-940 CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
GO ID Ontology Definition Evidence Reference
GO:0005102 Function Signaling receptor binding IEA
GO:0005515 Function Protein binding IPI 24120361, 28827714
GO:0005886 Component Plasma membrane IC 20554964
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610925 18358 ENSG00000163702
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8NAC3
Protein name Interleukin-17 receptor C (IL-17 receptor C) (IL-17RC) (Interleukin-17 receptor homolog) (IL17Rhom) (Interleukin-17 receptor-like protein) (IL-17RL) (ZcytoR14)
Protein function Receptor for IL17A and IL17F, major effector cytokines of innate and adaptive immune system involved in antimicrobial host defense and maintenance of tissue integrity (By similarity). Receptor for IL17A and IL17F, major effector cytokines of inn
PDB 6HG4 , 6HG9 , 6HGA , 7UWN , 7ZAN
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15037 IL17_R_N 142 530 Interleukin-17 receptor extracellular region Family
PF08357 SEFIR 584 737 SEFIR domain Family
Tissue specificity TISSUE SPECIFICITY: Expressed in prostate, skeletal muscle, kidney and placenta (at protein level) (PubMed:11706037). Expressed in brain, cartilage, colon, heart, intestine, kidney, liver, lung, muscle, placenta, and prostate (PubMed:11706037). Also detec
Sequence
Sequence length 791
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
20
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Candidiasis, familial, 9 Likely pathogenic; Pathogenic rs755012426, rs1057518751, rs143600903 RCV003227540
RCV000412591
RCV000412524
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
Adrenocortical carcinoma, hereditary Benign; Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Cervical cancer Benign; Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Colon adenocarcinoma Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Familial cancer of breast Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Age related macular degeneration Age-related macular degeneration BEFREE 23177625, 24373284, 24780906
★☆☆☆☆
Found in Text Mining only
Androgen-Insensitivity Syndrome Androgen-Insensitivity Syndrome BEFREE 22999050
★☆☆☆☆
Found in Text Mining only
Arthritis Rheumatoid Rheumatoid arthritis Pubtator 29584788, 37926850 Associate
★☆☆☆☆
Found in Text Mining only
Bladder Neoplasm Bladder Neoplasm BEFREE 27716046
★☆☆☆☆
Found in Text Mining only
Bladder polyp Bladder polyp BEFREE 27716046
★☆☆☆☆
Found in Text Mining only
Bullous pemphigoid Bullous Pemphigoid BEFREE 31572359
★☆☆☆☆
Found in Text Mining only
Capillary malformation (disorder) Capillary malformation GENOMICS_ENGLAND_DG 29076381
★☆☆☆☆
Found in Text Mining only
Carcinoma of bladder Bladder carcinoma BEFREE 27716046
★☆☆☆☆
Found in Text Mining only
Cerebral Infarction Ischemic stroke Pubtator 31481525 Associate
★☆☆☆☆
Found in Text Mining only
Cheilitis Cheilitis HPO_DG
★☆☆☆☆
Found in Text Mining only