RecName: Full=Sodium channel regulatory subunit beta-1; Flags: Precurs - Protein

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Impact of rs1805127 and rs55742440 Variants on Atrial Remodeling in Hypertrophic Cardiomyopathy Patients with Atrial Fibrillation: A Romanian Cohort Study. [Int J Mol Sci. 2023]
Impact of rs1805127 and rs55742440 Variants on Atrial Remodeling in Hypertrophic Cardiomyopathy Patients with Atrial Fibrillation: A Romanian Cohort Study.
Popa-Fotea NM, Oprescu N, Scafa-Udriste A, Micheu MM. Int J Mol Sci. 2023 Dec 8; 24(24). Epub 2023 Dec 8.
A founder event causing a dominant childhood epilepsy survives 800 years through weak selective pressure. [Am J Hum Genet. 2022]
A founder event causing a dominant childhood epilepsy survives 800 years through weak selective pressure.
Grinton BE, Robertson E, Fearnley LG, Scheffer IE, Marson AG, O'Brien TJ, Pickrell WO, Rees MI, Sisodiya SM, Balding DJ, et al. Am J Hum Genet. 2022 Nov 3; 109(11):2080-2087. Epub 2022 Oct 25.
Homozygous SCN1B variants causing early infantile epileptic encephalopathy 52 affect voltage-gated sodium channel function. [Epilepsia. 2021]
Homozygous SCN1B variants causing early infantile epileptic encephalopathy 52 affect voltage-gated sodium channel function.
Scala M, Efthymiou S, Sultan T, De Waele J, Panciroli M, Salpietro V, Maroofian R, Striano P, Van Petegem F, Houlden H, et al. Epilepsia. 2021 Jun; 62(6):e82-e87. Epub 2021 Apr 26.

RefSeq genomic sequence
See the genomic reference sequence for the SCN1B gene (NG_013359.1).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the SCN1B gene.

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Q07699 [Domain Mapping of Disease Mut...]
Q07699
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
Reactome [Reactome]
Reactome
reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome
reagents [ExactAntigen/Labome]
reagents
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Protein