ENSG00000163702


Homo sapiens

Features
Gene ID: ENSG00000163702
  
Biological name :IL17RC
  
Synonyms : IL17RC / interleukin 17 receptor C / Q8NAC3
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 3
Strand: 1
Band: p25.3
Gene start: 9917074
Gene end: 9933630
  
Corresponding Affymetrix probe sets: 221926_s_at (Human Genome U133 Plus 2.0 Array)   224514_x_at (Human Genome U133 Plus 2.0 Array)   64440_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000410834
Ensembl peptide - ENSP00000407894
Ensembl peptide - ENSP00000412777
Ensembl peptide - ENSP00000432564
Ensembl peptide - ENSP00000414609
Ensembl peptide - ENSP00000413914
Ensembl peptide - ENSP00000295981
Ensembl peptide - ENSP00000373323
Ensembl peptide - ENSP00000384969
Ensembl peptide - ENSP00000387675
Ensembl peptide - ENSP00000390080
Ensembl peptide - ENSP00000394996
Ensembl peptide - ENSP00000395315
Ensembl peptide - ENSP00000396064
Ensembl peptide - ENSP00000399396
Ensembl peptide - ENSP00000401128
NCBI entrez gene - 84818     See in Manteia.
OMIM - 610925
RefSeq - XM_017007349
RefSeq - XM_017007332
RefSeq - XM_017007333
RefSeq - XM_017007334
RefSeq - XM_017007335
RefSeq - XM_017007336
RefSeq - XM_017007337
RefSeq - XM_017007338
RefSeq - XM_017007339
RefSeq - XM_017007340
RefSeq - XM_017007341
RefSeq - XM_017007342
RefSeq - XM_017007343
RefSeq - XM_017007344
RefSeq - XM_017007345
RefSeq - XM_017007346
RefSeq - XM_017007347
RefSeq - XM_017007348
RefSeq - NM_001203263
RefSeq - NM_001203264
RefSeq - NM_001203265
RefSeq - NM_032732
RefSeq - NM_153460
RefSeq - NM_153461
RefSeq - XM_017007326
RefSeq - XM_017007327
RefSeq - XM_017007328
RefSeq - XM_017007329
RefSeq - XM_017007330
RefSeq - XM_017007331
RefSeq Peptide - NP_703190
RefSeq Peptide - NP_703191
RefSeq Peptide - NP_001190194
RefSeq Peptide - NP_116121
RefSeq Peptide - NP_001190192
RefSeq Peptide - NP_001190193
swissprot - F8WE27
swissprot - F8WEG5
swissprot - C9K0M1
swissprot - Q8NAC3
swissprot - A8K3Q5
swissprot - G3V177
swissprot - C9JSZ3
swissprot - B4DI24
swissprot - F8WB43
swissprot - F8WC09
swissprot - F8WD65
Ensembl - ENSG00000163702
  
Related genetic diseases (OMIM): 616445 - Candidiasis, familial, 9, 616445
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 FO904970.1ENSDARG00000105863Danio rerio
 il17rcENSDARG00000099902Danio rerio
 Il17rcENSMUSG00000030281Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR013568  SEFIR domain
 IPR027841  Interleukin-17 receptor C/E, N-terminal


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0050832 defense response to fungus IEA
 biological_processGO:0071621 granulocyte chemotaxis IEA
 biological_processGO:0097400 interleukin-17-mediated signaling pathway TAS
 biological_processGO:1900017 positive regulation of cytokine production involved in inflammatory response IEA
 biological_processGO:2000778 positive regulation of interleukin-6 secretion IEA
 cellular_componentGO:0005886 plasma membrane TAS
 cellular_componentGO:0005887 integral component of plasma membrane IBA
 cellular_componentGO:0009986 cell surface IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 molecular_functionGO:0005102 signaling receptor binding IEA
 molecular_functionGO:0030368 interleukin-17 receptor activity IDA


Pathways (from Reactome)
Pathway description
Interleukin-17 signaling


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0000010 Recurrent urinary tract infections "Repeated infections of the urinary tract." [HPO:curators]
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 HP:0000142 Abnormality of the vagina 
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 HP:0000504 Abnormality of vision "Abnormality of eyesight (visual perception)." [HPO:curators]
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 HP:0000682 Abnormality of dental enamel "An abnormality of the dental enamel, which is the external layer of the teeth, being a highly mineralized substance consisting primarily of hydroxylapatite." [HPO:curators]
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 HP:0000790 Hematuria "The presence of blood in the urine. Hematuria may be gross hematuria (visible to the naked eye) or microscopic hematuria (detected by dipstick or microscopic examination of the urine)." [HPO:curators]
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 HP:0000962 Hyperkeratosis "Hyperkeratosis is thickening of the outer layer of the skin, the stratum corneum, which is composed of large, polyhedral, plate-like envelopes filled with keratin which are the dead cells that have migrated up from the stratum granulosum." [HPO:curators]
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 HP:0000988 Skin rash 
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 HP:0000989 Pruritus "Pruritus is an itch or a sensation that makes a person want to scratch. This term refers to an abnormally increased disposition to experience pruritus." [HPO:curators]
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 HP:0001231 Abnormality of the fingernails "An abnormality of the `fingernails` (FMA:54327)." [HPO:probinson]
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 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
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 HP:0001821 Broad nails 
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 HP:0002105 Hemoptysis "Coughing up (expectoration) of blood or blood-streaked sputum from the larynx, trachea, bronchi, or lungs." [HPO:curators]
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 HP:0002205 Recurrent respiratory infections 
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 HP:0004306 Abnormality of the endocardium "An abnormality of the `endocardium` (FMA:7280)." [HPO:probinson]
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 HP:0004370 Abnormality of temperature regulation 
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 HP:0008388 Abnormality of the toenails 
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 HP:0008872 Feeding problems in infancy 
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 HP:0010783 Erythema "Redness of the skin, caused by hyperemia of the capillaries in the lower layers of the skin." [HPO:probinson]
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 HP:0011107 Recurrent aphthous stomatitis "Recurrent episodes of ulceration of the oral mucosa." [HPO:probinson]
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 HP:0012115 Hepatitis "Inflammation of the liver." [HPO:probinson]
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 HP:0012203 Onychomycosis "A fungal infection of the toenails or fingernails that tends to cause the nails to thicken, discolor, disfigure, and split." [HPO:probinson]
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 HP:0012735 Cough "A sudden, audible expulsion of air from the lungs through a partially closed glottis, preceded by inhalation." [HPO:probinson]
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 HP:0030016 Dyspareunia "Recurrent or persistent genital pain associated with sexual intercourse." []
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 HP:0100825 Cheilitis "Inflammation of the lip." [HPO:sdoelken]
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 HP:0200034 skin papules "A circumscribed, solid elevation of skin with no visible fluid, varying in size from a pinhead to less than 10mm in diameter at the widest point." [HPO:SKOEHLER]
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 HP:0200042 skin ulcer "A discontinuity of the skin exhibiting complete loss of the epidermis and often portions of the dermis and even subcutaneous fat." [HPO:SKOEHLER]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000177663 IL17RA / Q96F46 / interleukin 17 receptor A  / complex
 ENSG00000112116 IL17F / Q96PD4 / interleukin 17F  / complex
 ENSG00000112115 IL17A / Q16552 / interleukin 17A  / complex






 

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