Entity Details

Primary name SCN2B_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionO60939
EntryNameSCN2B_HUMAN
FullNameSodium channel subunit beta-2
TaxID9606
Evidenceevidence at protein level
Length215
SequenceStatuscomplete
DateCreated2001-01-11
DateModified2021-06-02

Ontological Relatives

GenesSCN2B

GO terms

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GOName
GO:0001518 voltage-gated sodium channel complex
GO:0005244 voltage-gated ion channel activity
GO:0007268 chemical synaptic transmission
GO:0007399 nervous system development
GO:0017080 sodium channel regulator activity
GO:0035725 sodium ion transmembrane transport
GO:0045202 synapse
GO:0046684 response to pyrethroid
GO:0060048 cardiac muscle contraction
GO:0060371 regulation of atrial cardiac muscle cell membrane depolarization
GO:0086002 cardiac muscle cell action potential involved in contraction
GO:0086006 voltage-gated sodium channel activity involved in cardiac muscle cell action potential
GO:0086012 membrane depolarization during cardiac muscle cell action potential
GO:0086091 regulation of heart rate by cardiac conduction
GO:2000649 regulation of sodium ion transmembrane transporter activity

Subcellular Location

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Subcellular Location
Membrane

Domains

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DomainNameCategoryType
IPR000920 Myelin P0 protein-relatedFamilyFamily
IPR003599 Immunoglobulin subtypeDomainDomain
IPR007110 Immunoglobulin-like domainDomainDomain
IPR013106 Immunoglobulin V-set domainDomainDomain
IPR013783 Immunoglobulin-like foldFamilyHomologous superfamily
IPR029873 Sodium channel subunit beta-2FamilyFamily
IPR036179 Immunoglobulin-like domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
615378 OMIMAtrial fibrillation, familial, 14 (ATFB14)A familial form of atrial fibrillation, a common sustained cardiac rhythm disturbance. Atrial fibrillation is characterized by disorganized atrial electrical activity and ineffective atrial contraction promoting blood stasis in the atria and reduces ventricular filling. It can result in palpitations, syncope, thromboembolic stroke, and congestive heart failure. The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB00243 RanolazineDrugbanksmall molecule
DB00313 Valproic acidDrugbanksmall molecule
DB00776 OxcarbazepineDrugbanksmall molecule
DB00907 CocaineDrugbanksmall molecule
DB00909 ZonisamideDrugbanksmall molecule
DB05541 BrivaracetamDrugbanksmall molecule
DB13269 Dichlorobenzyl alcoholDrugbanksmall molecule
DB13961 Fish oilDrugbankbiotech

Interactions

0 interactions

InteractorPartnerSourcesPublicationsLink