ENSG00000100379


Homo sapiens

Features
Gene ID: ENSG00000100379
  
Biological name :KCTD17
  
Synonyms : KCTD17 / potassium channel tetramerization domain containing 17 / Q8N5Z5
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 22
Strand: 1
Band: q12.3
Gene start: 37051736
Gene end: 37063390
  
Corresponding Affymetrix probe sets: 1554566_at (Human Genome U133 Plus 2.0 Array)   205561_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000409116
Ensembl peptide - ENSP00000402434
Ensembl peptide - ENSP00000409638
Ensembl peptide - ENSP00000480699
Ensembl peptide - ENSP00000384391
Ensembl peptide - ENSP00000385096
NCBI entrez gene - 79734     See in Manteia.
OMIM - 616386
RefSeq - XM_011530377
RefSeq - NM_001282684
RefSeq - NM_001282685
RefSeq - NM_001282686
RefSeq - NM_024681
RefSeq - XM_005261741
RefSeq - XM_005261742
RefSeq - XM_005261743
RefSeq - XM_005261744
RefSeq - XM_011530374
RefSeq Peptide - NP_001269614
RefSeq Peptide - NP_001269615
RefSeq Peptide - NP_078957
RefSeq Peptide - NP_001269613
swissprot - B0QYB2
swissprot - Q8N5Z5
swissprot - H0Y731
swissprot - H7C323
swissprot - A0A087WX35
Ensembl - ENSG00000100379
  
Related genetic diseases (OMIM): 616398 - Dystonia 26, myoclonic, 616398
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
 kctd17ENSDARG00000056050Danio rerio
 KCTD17ENSGALG00000042419Gallus gallus
 Kctd17ENSMUSG00000033287Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
KCTD5 / Q9NXV2 / potassium channel tetramerization domain containing 5ENSG0000016797749
KCTD2 / Q14681 / potassium channel tetramerization domain containing 2ENSG0000018090146
KCTD9 / Q7L273 / potassium channel tetramerization domain containing 9ENSG0000010475622


Protein motifs (from Interpro)
Interpro ID Name
 IPR000210  BTB/POZ domain
 IPR003131  Potassium channel tetramerisation-type BTB domain
 IPR011333  SKP1/BTB/POZ domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0030030 cell projection organization IEA
 biological_processGO:0032469 endoplasmic reticulum calcium ion homeostasis IMP
 biological_processGO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process IMP
 biological_processGO:0045724 positive regulation of cilium assembly IMP
 biological_processGO:0051260 protein homooligomerization IEA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005783 endoplasmic reticulum IEA
 cellular_componentGO:0031463 Cul3-RING ubiquitin ligase complex IDA
 molecular_functionGO:0005515 protein binding IEA
 molecular_functionGO:0042802 identical protein binding IPI
 molecular_functionGO:0097602 cullin family protein binding IPI


Pathways (from Reactome)
Pathway description
No match


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]
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 HP:0000473 Torticollis 
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 HP:0000643 Blepharospasm "An involuntary recurrent spasm of both eyelids." [HPO:curators]
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 HP:0000716 Depression "A condition characterized by pervasive dysphoric mood, loss of interests, and inability to experience pleasure." [HPO:curators]
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 HP:0000722 Obsessive-compulsive disorder 
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 HP:0000739 Anxiety 
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 HP:0001260 Dysarthria "Dysarthric speech is a general description referring to a neurological speech disorder characterized by poor articulation. Depending on the involved neurological structures, dysarthria may be further classified as spastic, flaccid, ataxic, hyperkinetic and hypokinetic, or mixed." [HPO:curators]
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 HP:0001336 Myoclonus "Very brief, involuntary random muscular contractions occurring at rest, in response to sensory stimuli, or accompanying voluntary movements." [HPO:curators]
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 HP:0002356 Writer s cramp 
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 HP:0003676 Progressive disorder 
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 HP:0010531 Spinal myoclonus "Spinal myoclonus is generally due to a tumor, infection, injury, or degenerative process of the spinal cord, and is characterized by involuntary rhythmic muscle contractions, usually at a rate of more than one per second. Myoclonus occurs synchronously in several muscles and can be increased in severity and frequency by fatigue or stress, but is usually unaffected by sensory stimuli. Spinal myoclonus ceases during sleep or anesthesia." [HPO:curators]
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 HP:0012049 Laryngeal dystonia "A form of focal dystonia that affects the vocal cords, associated with involuntary contractions of the vocal cords causing interruptions of speech and affecting the voice quality and often leading to patterned, repeated breaks in speech." [HPO:probinson]
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 HP:0012075 Personality disorder "An abnormality of mental functioning affecting the personality and behavioural tendencies of an individual and characterized by a rigid and unhealthy pattern of thinking and behavior. The definition of a personal disorder implies that the abnormality is not the result of damage or insult to the brain or from another psychiatric disorder." [HPO:probinson]
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 HP:0025269 Panic attack "A sudden episode of intense fear in a situation in which there is no danger or apparent cause. The panic attack is accompanied by symptoms such as palpitations, sweating and chills or hot flushes. There may be a sensation of dyspnea (being out of breath), chest pain, or abdominal distress. Some indiviudals with panic attacks may experience depersonalization, a fear of going crazy, or a fear of dying." []
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 HP:0045084 Limb myoclonus 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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