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FLASH GENE
Symbol KCNQ3 contributors: mct/npt/pgu - updated : 15-07-2008
HGNC name potassium voltage-gated channel, KQT-like subfamily, member 3
HGNC id 6297
DNA
TYPE functioning gene
STRUCTURE 351.00 kb     15 Exon(s)
10 Kb 5' upstream gene genomic sequence study
regulatory sequence
MAPPING cloned Y linked N status provisional
RNA
TRANSCRIPTS type messenger
identificationnb exonstypebpproduct
ProteinkDaAAspecific expressionYearPubmed
15 - 3097 96.7 872 - 2008 18166285
EXPRESSION
Type restricted
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
Digestivemouth    
Nervousbraindiencephalonhypothalamus  
 brainforebraincerebral cortex  
 brainhindbraincerebellumcerebellar cortex 
Visualeye    
tissue
SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
Nervouscentral   
Nervousperipherous   
cells
SystemCellPubmedSpeciesStageRna symbol
Nervousneuron
cell lineage
cell lines
fluid/secretion
at STAGE
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
  • six membrane spanning domains
  • an hydrophobic pore (Ploop), flanked by TM domains 5 and 6, sensitive to changes in membrane potential
  • HOMOLOGY
    Homologene
    FAMILY
  • potassium channel family
  • KQT subfamily
  • CATEGORY transport channel
    SUBCELLULAR LOCALIZATION     plasma membrane
    text
  • located in or toward the apical membrane of the cells
  • basic FUNCTION
  • potassium voltage-gated channel, playing a critical role in the regulation of neuronal excitability
  • member of axonal Kv7 channels that are critically and uniquely required for determining the inherent spontaneous firing of hippocampal CA1 pyramids, independently of alterations in synaptic activity
  • role of a number of KCNQ channel members in controlling basal anion secretion in the airway epithelium
  • KCNQ2/3 channels could be an important regulator in neuronal apoptosis
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism
    signaling
    a component
  • M channel constituent (coassembling with KCNQ2 and KCNQ5)
  • INTERACTION
    DNA
    RNA
    small molecule
    protein
  • targeted to the axon initial segment of hippocampal neurons by association with ankyrin G
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s) EBN2 , EJM2
    Susceptibility to idiopathic epilepsy
    Variant & Polymorphism SNP missense variant p.Pro574Ser was detected in idiopathic epilepsy
    Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS