Scn3a Gene Summary [Mouse]

Predicted to enable calmodulin binding activity; sodium ion binding activity; and voltage-gated sodium channel activity. Involved in behavioral response to pain. Located in membrane and sarcoplasm. Is expressed in gut; heart; and nervous system. Human ortholog(s) of this gene implicated in developmental and epileptic encephalopathy 62 and familial focal epilepsy with variable foci 4. Orthologous to human SCN3A (sodium voltage-gated channel alpha subunit 3). [provided by Alliance of Genome Resources, Apr 2025]

Details

Type
Protein Coding
Official Symbol
Scn3a
Official Name
sodium channel, voltage-gated, type III, alpha [Source:MGI Symbol;Acc:MGI:98249]
Ensembl ID
ENSMUSG00000057182
Bio databases IDs NCBI: 20269 Ensembl: ENSMUSG00000057182
Aliases sodium channel, voltage-gated, type III, alpha
Synonyms DEE62, EIEE62, FFEVF4, Gm1000, LOC100360249, LOC100360303, NAC3, Nav1.3, SCIII, Scn2a, sodium channel, voltage-gated, type III, alpha, sodium channel, voltage-gated, type III, α, sodium voltage-gated channel alpha subunit 3, sodium voltage-gated channel α subunit 3
Species
Mouse, Mus musculus
OrthologiesHumanRat

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in mouse Scn3a often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • Sodium ion transport-associated
  • Voltage-dependent L-type calcium channel, IQ-associated
  • voltage-gated sodium channel
  • Cytoplasmic domain of voltage-gated Na+ ion channel
  • sodium channel
  • Ion transport protein
  • calmodulin binding
  • metal ion binding
  • protein binding
  • ion channel
  • Polycystin cation channel

Pathways

Biological processes and signaling networks where the Scn3a gene in mouse plays a role, providing insight into its function and relevance in health or disease.

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
binds
disease
  • amyotrophic lateral sclerosis
  • familial focal epilepsy with variable foci 4
  • bipolar disorder
  • partial seizure with secondary generalization
  • migraines
  • neurodevelopmental disorder
  • early infantile epileptic encephalopathy type 62
  • epilepsy
  • multiple system atrophy
  • spinocerebellar ataxia type 2
regulated by
role in cell
  • response by

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Plasma Membrane
  • detergent-soluble membrane fractions
  • cell surface
  • cellular membrane
  • sarcoplasm
  • perikaryon
  • axons

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the mouse Scn3a gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • regulation of cardiac muscle cell action potential involved in contraction
  • sodium ion transport
  • behavioral response to pain
  • sodium ion transmembrane transport

Cellular Component

Where in the cell the gene product is active
  • sarcoplasm
  • voltage-gated sodium channel complex

Molecular Function

What the gene product does at the molecular level
  • voltage-gated sodium channel activity

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.