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FLASH GENE
Symbol SCN4B contributors: mct/npt - updated : 11-09-2009
HGNC name sodium channel, voltage-gated, type IV, beta
HGNC id 10592
Location 11q23.3      Physical location : 118.004.093 - 118.023.630
DNA
TYPE functioning gene
STRUCTURE 19.44 kb     5 Exon(s)
10 Kb 5' upstream gene genomic sequence study
MAPPING cloned Y linked N status provisional
RNA
TRANSCRIPTS type messenger
identificationnb exonstypebpproduct
ProteinkDaAAspecific expressionYearPubmed
3 - 4177 - 94 - Medeiros-Domingo (2007)
4 - 4516 - 118 - Medeiros-Domingo (2007)
5 - 4579 - 228 - Medeiros-Domingo (2007)
EXPRESSION
Type widely
constitutive of
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
Nervousbrain    
 spinal cord    
cells
SystemCellPubmedSpeciesStageRna symbol
Nervousneuron
cell lineage
cell lines
fluid/secretion
at STAGE
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
  • a N-terminal signal peptide
  • a single transmembrane alpha helix
  • an extracellular domain with a single immunoglobulin-like fold, both necessary and sufficient for the modulation of Na(+) channel gating (McCormick 1999)
  • a small intracellular domain
  • conjugated GlycoP
    mono polymer heteromer
    HOMOLOGY
    Homologene
    FAMILY
    CATEGORY receptor membrane , transport channel
    SUBCELLULAR LOCALIZATION     plasma membrane
    basic FUNCTION
  • could alter the channel properties of SCN4A
  • has little effect on the channel kinetics of cardiac SCN5A
  • may affect both protein-protein interactions and physiological functions of several sodium channel alpha subunits
  • play a critical role in regulation of neuronal excitability (Ferreira 2006)
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism
    signaling
    a component
    INTERACTION
    DNA
    RNA
    small molecule
    protein
  • may interact with SCN4A
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s)
    Other morbid association(s)
    TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
    constitutional        
    a missense mutation cosegegating with LQTS in a 3-generation pedigree (Medeiros-Domingo et al,2007)
    Susceptibility
    Variant & Polymorphism
    Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS