ENSMUSG00000028631


Mus musculus

Features
Gene ID: ENSMUSG00000028631
  
Biological name :Kcnq4
  
Synonyms : Kcnq4 / Potassium voltage-gated channel subfamily KQT member 4 / Q9JK97
  
Possible biological names infered from orthology : P56696 / potassium voltage-gated channel subfamily Q member 4
  
Species: Mus musculus
  
Chr. number: 4
Strand: -1
Band: D2.2
Gene start: 120696138
Gene end: 120748612
  
Corresponding Affymetrix probe sets: 10515960 (MoGene1.0st)   1435721_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000030376
NCBI entrez gene - 60613     See in Manteia.
MGI - MGI:1926803
RefSeq - XM_011240583
RefSeq - NM_001081142
RefSeq - XM_006503255
RefSeq - XM_011240582
RefSeq Peptide - NP_001074611
swissprot - Q9JK97
Ensembl - ENSMUSG00000028631
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 kcnq4ENSDARG00000089490Danio rerio
 KCNQ4ENSGALG00000038708Gallus gallus
 KCNQ4ENSG00000117013Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Kcnq5 / Q9JK45 / Potassium voltage-gated channel subfamily KQT member 5 / Q9NR82* / potassium voltage-gated channel subfamily Q member 5*ENSMUSG0000002803358
Kcnq2 / potassium voltage-gated channel subfamily KQT member 2 isoform 13 / O43526* / potassium voltage-gated channel subfamily Q member 2*ENSMUSG0000001634652
Kcnq3 / Q8K3F6 / Potassium voltage-gated channel subfamily KQT member 3 / O43525* / potassium voltage-gated channel subfamily Q member 3*ENSMUSG0000005625845
Kcnq1 / P97414 / Potassium voltage-gated channel subfamily KQT member 1 / P51787* / potassium voltage-gated channel subfamily Q member 1*ENSMUSG0000000954533


Protein motifs (from Interpro)
Interpro ID Name
 IPR003937  Potassium channel, voltage dependent, KCNQ
 IPR005821  Ion transport domain
 IPR013821  Potassium channel, voltage dependent, KCNQ, C-terminal
 IPR015573  Potassium channel, voltage dependent, KCNQ4
 IPR028325  Voltage-gated potassium channel


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006811 ion transport IEA
 biological_processGO:0006813 potassium ion transport IMP
 biological_processGO:0007605 sensory perception of sound IEA
 biological_processGO:0034765 regulation of ion transmembrane transport IEA
 biological_processGO:0042472 inner ear morphogenesis IMP
 biological_processGO:0055085 transmembrane transport IEA
 biological_processGO:0071805 potassium ion transmembrane transport IEA
 cellular_componentGO:0005886 plasma membrane IEA
 cellular_componentGO:0008076 voltage-gated potassium channel complex IEA
 cellular_componentGO:0009925 basal plasma membrane IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IBA
 molecular_functionGO:0005216 ion channel activity IEA
 molecular_functionGO:0005244 voltage-gated ion channel activity IEA
 molecular_functionGO:0005249 voltage-gated potassium channel activity IMP
 molecular_functionGO:0005267 potassium channel activity IEA


Pathways (from Reactome)
Pathway description
Voltage gated Potassium channels


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0004404 cochlear outer hair cell degeneration "degeneration or loss of the columnar outer hair sensory cells of the organ of Corti" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Chmtm1.1Seab/Y,Tg(Six3-cre)69Frty/0
Genetic Background: involves: 129X1/SvJ * C57BL/6 * DBA/2

Allelic Composition: Kcnq4tm1.2Tjj/Kcnq4tm1.2Tjj
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Kcnq4tm1.2Tjj/Kcnq4+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0004434 abnormal cochlear outer hair cell physiology "anomalies in processes pertinent to the function of cochlear OHCs which are known to enhance the performance of the cochlea, both qualitatively (increased selectivity) and quantitatively (increased sensitivity); in addition to the mechanoelectric transduction required for auditory sensation, OHCs also perform electromechanical transduction, whereby transmembrane voltage drives rapid changes in the length and stiffness of OHCs at audio frequencies in vitro (electromotility)" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Kcnq4tm1.2Tjj/Kcnq4tm1.2Tjj
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0004737 absent distortion product otoacoustic emissions "failure to create mechanical distortions in the inner ear when two primary tones are presented, indicating failure of outer hair cells to amplify basilar membrane motion" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Kcnq4tm1.2Tjj/Kcnq4tm1.2Tjj
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0004740 sensorineural hearing loss "a form of progressive hearing loss due to a lesion of the auditory division of cranial nerve VIII or the inner ear" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Chmtm1.1Seab/Y,Tg(Six3-cre)69Frty/0
Genetic Background: involves: 129X1/SvJ * C57BL/6 * DBA/2

Allelic Composition: Kcnq4tm1.2Tjj/Kcnq4tm1.2Tjj
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Kcnq4tm1.2Tjj/Kcnq4+
Genetic Background: involves: 129/Sv * C57BL/6

 MP:0011967 increased or absent threshold for auditory brainstem response "increase in the value at which one or more sound frequencies or broadband clicks first elicits a recordable response generated by electrical activity of neurons in the ascending auditory system, or complete lack of a recordable response at any frequency or broadband click" [MGI:csmith]
Show

Allelic Composition: Chmtm1.1Seab/Y,Tg(Six3-cre)69Frty/0
Genetic Background: involves: 129X1/SvJ * C57BL/6 * DBA/2

Allelic Composition: Kcnq4tm1.2Tjj/Kcnq4tm1.2Tjj
Genetic Background: involves: 129/Sv * C57BL/6

Allelic Composition: Kcnq4tm1.2Tjj/Kcnq4+
Genetic Background: involves: 129/Sv * C57BL/6

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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