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SCN1B

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Protein-coding gene in the species Homo sapiens
SCN1B
Identifiers
AliasesSCN1B, ATFB13, BRGDA5, GEFSP1, sodium voltage-gated channel beta subunit 1, EIEE52, DEE52
External IDsOMIM: 600235; MGI: 98247; HomoloGene: 810; GeneCards: SCN1B; OMA:SCN1B - orthologs
Gene location (Human)
Chromosome 19 (human)
Chr.Chromosome 19 (human)
Chromosome 19 (human)Genomic location for SCN1BGenomic location for SCN1B
Band19q13.11Start35,030,470 bp
End35,040,449 bp
Gene location (Mouse)
Chromosome 7 (mouse)
Chr.Chromosome 7 (mouse)
Chromosome 7 (mouse)Genomic location for SCN1BGenomic location for SCN1B
Band7 B1|7 19.3 cMStart30,815,949 bp
End30,826,428 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • primary visual cortex

  • right hemisphere of cerebellum

  • gastrocnemius muscle

  • right frontal lobe

  • muscle of thigh

  • skeletal muscle tissue

  • dorsolateral prefrontal cortex

  • Brodmann area 9

  • superior frontal gyrus

  • prefrontal cortex
Top expressed in
  • superior frontal gyrus

  • primary visual cortex

  • muscle of thigh

  • dentate gyrus of hippocampal formation granule cell

  • cerebellar cortex

  • extensor digitorum longus muscle

  • CA3 field

  • perirhinal cortex

  • triceps brachii muscle

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

6324

20266

Ensembl

ENSG00000105711

ENSMUSG00000019194

UniProt

Q07699

P97952

RefSeq (mRNA)

NM_001037
NM_199037
NM_001321605

NM_011322

RefSeq (protein)

NP_001028
NP_001308534
NP_950238

NP_035452
NP_001389263

Location (UCSC)Chr 19: 35.03 – 35.04 MbChr 7: 30.82 – 30.83 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Sodium channel subunit beta-1 is a protein that in humans is encoded by the SCN1B gene.

Voltage-gated sodium channels are essential for the generation and propagation of action potentials in striated muscle and neuronal tissues. Biochemically, they consist of a large alpha subunit and 1 or 2 smaller beta subunits, such as SCN1B. The alpha subunit alone can exhibit all the functional attributes of a voltage-gated Na+ channel, but requires a beta-1 subunit for normal inactivation kinetics.

Clinical significance

Mutation in the SCN1B gene are associated with disorders such as Brugada syndrome, Dravet Syndrome, and GEFS.

See also

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000105711Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000019194Ensembl, 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. McClatchey AI, Cannon SC, Slaugenhaupt SA, Gusella JF (Sep 1993). "The cloning and expression of a sodium channel beta 1-subunit cDNA from human brain". Hum Mol Genet. 2 (6): 745–9. doi:10.1093/hmg/2.6.745. PMID 8394762.
  6. ^ "Entrez Gene: SCN1B sodium channel, voltage-gated, type I, beta".

Further reading

External links

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

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


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