ENSG00000184156


Homo sapiens

Features
Gene ID: ENSG00000184156
  
Biological name :KCNQ3
  
Synonyms : KCNQ3 / O43525 / potassium voltage-gated channel subfamily Q member 3
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 8
Strand: -1
Band: q24.22
Gene start: 132120858
Gene end: 132481019
  
Corresponding Affymetrix probe sets: 1557042_at (Human Genome U133 Plus 2.0 Array)   206573_at (Human Genome U133 Plus 2.0 Array)   228579_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000373648
Ensembl peptide - ENSP00000492691
Ensembl peptide - ENSP00000491940
Ensembl peptide - ENSP00000491165
Ensembl peptide - ENSP00000482510
Ensembl peptide - ENSP00000429799
Ensembl peptide - ENSP00000428790
NCBI entrez gene - 3786     See in Manteia.
OMIM - 602232
RefSeq - XM_017013400
RefSeq - NM_001204824
RefSeq - NM_004519
RefSeq - XM_005250914
RefSeq - XM_006716555
RefSeq - XM_011517026
RefSeq Peptide - NP_004510
RefSeq Peptide - NP_001191753
swissprot - A0A1W2PNZ2
swissprot - A0A087WZB4
swissprot - A0A1W2PRN8
swissprot - E7ET42
swissprot - O43525
swissprot - A0A1W2PQ71
Ensembl - ENSG00000184156
  
Related genetic diseases (OMIM): 121201 - Seizures, benign neonatal, 2, 121201
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
 kcnq3ENSDARG00000060085Danio rerio
 KCNQ3ENSGALG00000037626Gallus gallus
 Kcnq3ENSMUSG00000056258Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
KCNQ2 / O43526 / potassium voltage-gated channel subfamily Q member 2ENSG0000007504347
KCNQ5 / Q9NR82 / potassium voltage-gated channel subfamily Q member 5ENSG0000018576042
KCNQ4 / P56696 / potassium voltage-gated channel subfamily Q member 4ENSG0000011701335
KCNQ1 / P51787 / potassium voltage-gated channel subfamily Q member 1ENSG0000005391827


Protein motifs (from Interpro)
Interpro ID Name
 IPR003937  Potassium channel, voltage dependent, KCNQ
 IPR003948  Potassium channel, voltage dependent, KCNQ3
 IPR005821  Ion transport domain
 IPR013821  Potassium channel, voltage dependent, KCNQ, C-terminal
 IPR020969  Ankyrin-G binding site
 IPR028325  Voltage-gated potassium channel


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006811 ion transport IEA
 biological_processGO:0006813 potassium ion transport IEA
 biological_processGO:0007268 chemical synaptic transmission TAS
 biological_processGO:0034765 regulation of ion transmembrane transport IEA
 biological_processGO:0055085 transmembrane transport IEA
 biological_processGO:0060081 membrane hyperpolarization IEA
 biological_processGO:0071805 potassium ion transmembrane transport IEA
 cellular_componentGO:0005886 plasma membrane ISS
 cellular_componentGO:0005887 integral component of plasma membrane IDA
 cellular_componentGO:0008076 voltage-gated potassium channel complex IEA
 cellular_componentGO:0009986 cell surface IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0033268 node of Ranvier ISS
 cellular_componentGO:0043194 axon initial segment ISS
 molecular_functionGO:0005216 ion channel activity IEA
 molecular_functionGO:0005244 voltage-gated ion channel activity IEA
 molecular_functionGO:0005249 voltage-gated potassium channel activity IEA
 molecular_functionGO:0005267 potassium channel activity IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0005516 calmodulin binding IDA


Pathways (from Reactome)
Pathway description
Voltage gated Potassium channels
Interaction between L1 and Ankyrins


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:0000490 Deep set eyes 
Show

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

 HP:0000738 Hallucinations 
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:0001252 Muscular hypotonia "Muscular hypotonia is an abnormally low muscle tone (the amount of tension or resistance to movement in a muscle), often involving reduced muscle strength. Hypotonia is characterized by a diminished resistance to passive stretching." [HPO:curators]
Show

 HP:0001266 Choreoathetosis 
Show

 HP:0001276 Hypertonia 
Show

 HP:0001336 Myoclonus "Very brief, involuntary random muscular contractions occurring at rest, in response to sensory stimuli, or accompanying voluntary movements." [HPO:curators]
Show

 HP:0002017 Nausea and vomiting 
Show

 HP:0002069 Generalized tonic-clonic seizures "Generalized tonic-clonic seizures are `generalized seizures` (HP:0002197) in which the patient suddenly loses conciousness, the eyes roll back, and the entire body musculature undergoes tonic contractions. In the clonic phase of the seizure, there are rhythmic contractions of the musculature alternating with relaxation of all muscle groups. Loss of sphincter control during the seizure is common. This form of seizure was formerly commonly called grand mal seizure." [HPO:curators]
Show

 HP:0002076 Migraine 
Show

 HP:0002266 Focal clonic seizures 
Show

 HP:0002354 Memory impairment 
Show

 HP:0002357 Dysphasia 
Show

 HP:0004372 Reduced consciousness/confusion 
Show

 HP:0012378 Fatigue "A subjective feeling of tiredness characterized by a lack of energy and motivation." [HPO:probinson]
Show

 HP:0012534 Dysesthesia "Abnormal sensations with no apparent physical cause that are painful or unpleasant." [ORCID:0000-0001-5208-3432]
Show

 HP:0100543 Cognitive impairment "Abnormality in the process of thought including the ability to process information." [HPO:sdoelken]
Show

 HP:0100660 Dyskinesis "A movement disorder which consists of effects including diminished voluntary movements and the presence of involuntary movements." [HPO:sdoelken]
Show

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000145362 ANK2 / Q01484 / ankyrin 2  / reaction / complex
 ENSG00000029534 ANK1 / P16157 / ankyrin 1  / complex / reaction
 ENSG00000163531 NFASC / O94856 / neurofascin  / reaction / complex
 ENSG00000184009 ACTG1 / P63261 / actin gamma 1  / reaction / complex
 ENSG00000075624 ACTB / P60709 / actin beta  / complex / reaction
 ENSG00000197694 Q13813 / SPTAN1 / spectrin alpha, non-erythrocytic 1  / complex / reaction
 ENSG00000091129 NRCAM / Q92823 / neuronal cell adhesion molecule  / complex / reaction
 ENSG00000163554 SPTA1 / P02549 / spectrin alpha, erythrocytic 1  / complex / reaction






 

0 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