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SCN3A

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Protein-coding gene in humans
SCN3A
Identifiers
AliasesSCN3A, NAC3, Nav1.3, sodium voltage-gated channel alpha subunit 3, FFEVF4, EIEE62, DEE62
External IDsOMIM: 182391; MGI: 98249; HomoloGene: 56005; GeneCards: SCN3A; OMA:SCN3A - orthologs
Gene location (Human)
Chromosome 2 (human)
Chr.Chromosome 2 (human)
Chromosome 2 (human)Genomic location for SCN3AGenomic location for SCN3A
Band2q24.3Start165,087,526 bp
End165,204,050 bp
Gene location (Mouse)
Chromosome 2 (mouse)
Chr.Chromosome 2 (mouse)
Chromosome 2 (mouse)Genomic location for SCN3AGenomic location for SCN3A
Band2 C1.3|2 38.55 cMStart65,287,462 bp
End65,397,971 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • endothelial cell

  • middle temporal gyrus

  • entorhinal cortex

  • Brodmann area 23

  • orbitofrontal cortex

  • Region I of hippocampus proper

  • postcentral gyrus

  • Brodmann area 46

  • cerebellar vermis

  • superior frontal gyrus
Top expressed in
  • superior cervical ganglion

  • habenula

  • dorsal striatum

  • endothelial cell of lymphatic vessel

  • dorsomedial hypothalamic nucleus

  • ventromedial nucleus

  • piriform cortex

  • paraventricular nucleus of hypothalamus

  • trigeminal ganglion

  • ventral tegmental area
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

6328

20269

Ensembl

ENSG00000153253

ENSMUSG00000057182

UniProt

Q9NY46

A2ASI5

RefSeq (mRNA)

NM_001081676
NM_001081677
NM_006922

NM_018732
NM_001355166
NM_001355167
NM_001355168
NM_001355169

NM_001355170
NM_001355171

RefSeq (protein)

NP_001075145
NP_001075146
NP_008853

NP_001342095
NP_001342096
NP_001342097
NP_001342098
NP_001342099

NP_001342100
NP_061202

Location (UCSC)Chr 2: 165.09 – 165.2 MbChr 2: 65.29 – 65.4 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Sodium channel, voltage-gated, type III, alpha subunit (SCN3A) is a protein that in humans is encoded by the SCN3A gene.

Function

Voltage-gated sodium channels are transmembrane glycoprotein complexes composed of a large alpha subunit with 24 transmembrane domains and one or more regulatory beta subunits. They are responsible for the generation and propagation of action potentials in neurons and muscle. This gene encodes one member of the sodium channel alpha subunit gene family, and is found in a cluster of five alpha subunit genes on chromosome 2. Multiple transcript variants encoding different isoforms have been found for this gene.

SCN3A is involved in gyrification – the folding of the human cerebral cortex, and affects speech production brain areas.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000153253Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000057182Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "UniProt". www.uniprot.org. Retrieved 24 July 2022.
  6. ^ "Entrez Gene: SCN3A sodium channel, voltage-gated, type III, alpha subunit".
  7. Smith RS, Kenny CJ, Ganesh V, Jang A, Borges-Monroy R, Partlow JN, et al. (September 2018). "Sodium Channel SCN3A (NaV1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development". Neuron. 99 (5): 905–913.e7. doi:10.1016/j.neuron.2018.07.052. PMC 6226006. PMID 30146301.

Further reading

External links

PDB gallery
  • 1byy: SODIUM CHANNEL IIA INACTIVATION GATE 1byy: SODIUM CHANNEL IIA INACTIVATION GATE
Membrane transport protein: ion channels (TC 1A)
Ca: Calcium channel
Ligand-gated
Voltage-gated
Na: Sodium channel
Constitutively active
Proton-gated
Voltage-gated
K: Potassium channel
Calcium-activated
Inward-rectifier
Tandem pore domain
Voltage-gated
Miscellaneous
Cl: Chloride channel
H: Proton channel
M: CNG cation channel
M: TRP cation channel
H2O (+ solutes): Porin
Cytoplasm: Gap junction
By gating mechanism
Ion channel class
see also disorders

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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