ENSG00000112116


Homo sapiens

Features
Gene ID: ENSG00000112116
  
Biological name :IL17F
  
Synonyms : IL17F / interleukin 17F / Q96PD4
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 6
Strand: -1
Band: p12.2
Gene start: 52236681
Gene end: 52244537
  
Corresponding Affymetrix probe sets: 234408_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000337432
NCBI entrez gene - 112744     See in Manteia.
OMIM - 606496
RefSeq - NM_052872
RefSeq - XM_011514276
RefSeq Peptide - NP_443104
swissprot - Q96PD4
Ensembl - ENSG00000112116
  
Related genetic diseases (OMIM): 613956 - ?Candidiasis, familial, 6, autosomal dominant, 613956
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
 il17a/f1ENSDARG00000043933Danio rerio
 il17a/f3ENSDARG00000041976Danio rerio
 ENSGALG00000016677Gallus gallus
 IL17AENSGALG00000016678Gallus gallus
 Il17fENSMUSG00000041872Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
IL17A / Q16552 / interleukin 17AENSG0000011211541


Protein motifs (from Interpro)
Interpro ID Name
 IPR010345  Interleukin-17 family
 IPR020440  Interleukin-17, chordata
 IPR029034  Cystine-knot cytokine


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006954 inflammatory response IEA
 biological_processGO:0010469 regulation of signaling receptor activity IEA
 biological_processGO:0016525 negative regulation of angiogenesis IDA
 biological_processGO:0017015 regulation of transforming growth factor beta receptor signaling pathway IDA
 biological_processGO:0019221 cytokine-mediated signaling pathway TAS
 biological_processGO:0042089 cytokine biosynthetic process IDA
 biological_processGO:0042109 lymphotoxin A biosynthetic process IDA
 biological_processGO:0045076 regulation of interleukin-2 biosynthetic process IDA
 biological_processGO:0045408 regulation of interleukin-6 biosynthetic process IDA
 biological_processGO:0045414 regulation of interleukin-8 biosynthetic process IDA
 biological_processGO:0045423 regulation of granulocyte macrophage colony-stimulating factor biosynthetic process IDA
 biological_processGO:0045944 positive regulation of transcription by RNA polymerase II IEA
 biological_processGO:0051216 cartilage development IDA
 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:0005576 extracellular region TAS
 cellular_componentGO:0005615 extracellular space IEA
 molecular_functionGO:0005125 cytokine activity IDA
 molecular_functionGO:0005126 cytokine receptor binding IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0019955 cytokine binding IDA
 molecular_functionGO:0042803 protein homodimerization activity IDA


Pathways (from Reactome)
Pathway description
Interleukin-17 signaling
Interleukin-4 and Interleukin-13 signaling


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000006 Autosomal dominant 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 heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators]
Show

 HP:0000010 Recurrent urinary tract infections "Repeated infections of the urinary tract." [HPO:curators]
Show

 HP:0000142 Abnormality of the vagina 
Show

 HP:0000504 Abnormality of vision "Abnormality of eyesight (visual perception)." [HPO:curators]
Show

 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]
Show

 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]
Show

 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]
Show

 HP:0000988 Skin rash 
Show

 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]
Show

 HP:0001231 Abnormality of the fingernails "An abnormality of the `fingernails` (FMA:54327)." [HPO:probinson]
Show

 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]
Show

 HP:0001821 Broad nails 
Show

 HP:0002105 Hemoptysis "Coughing up (expectoration) of blood or blood-streaked sputum from the larynx, trachea, bronchi, or lungs." [HPO:curators]
Show

 HP:0002205 Recurrent respiratory infections 
Show

 HP:0002728 Chronic mucocutaneous candidiasis 
Show

 HP:0004306 Abnormality of the endocardium "An abnormality of the `endocardium` (FMA:7280)." [HPO:probinson]
Show

 HP:0004370 Abnormality of temperature regulation 
Show

 HP:0008388 Abnormality of the toenails 
Show

 HP:0008872 Feeding problems in infancy 
Show

 HP:0010783 Erythema "Redness of the skin, caused by hyperemia of the capillaries in the lower layers of the skin." [HPO:probinson]
Show

 HP:0012115 Hepatitis "Inflammation of the liver." [HPO:probinson]
Show

 HP:0012735 Cough "A sudden, audible expulsion of air from the lungs through a partially closed glottis, preceded by inhalation." [HPO:probinson]
Show

 HP:0030016 Dyspareunia "Recurrent or persistent genital pain associated with sexual intercourse." []
Show

 HP:0100825 Cheilitis "Inflammation of the lip." [HPO:sdoelken]
Show

 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]
Show

 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]
Show

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000177663 IL17RA / Q96F46 / interleukin 17 receptor A  / complex
 ENSG00000112116 IL17F / Q96PD4 / interleukin 17F  / complex
 ENSG00000163702 IL17RC / Q8NAC3 / interleukin 17 receptor C  / complex
 ENSG00000112115 IL17A / Q16552 / interleukin 17A  / complex






 

1 s.

 
External programs and data are copyrighted by and are the property of their respective authors.
The Manteia system, data and analyses are provided "as is" with no warranties, expressed or implied as to capabilities or accuracy. User assumes the entire risk as to the results and performance of the software, data and documentation


                   


© Olivier Tassy / Olivier Pourquie 2007-2024
contact: otassy@igbmc.fr