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Everything about SCN3B
Protein-coding gene in the species Homo sapiens
Sodium channel subunit beta-3 is a protein that in humans is encoded by the SCN3B gene. Two alternatively spliced variants, encoding the same protein, have been identified. Wikipedia ā
š§ Start here: a 6-step reading path
- Read the overview: SCN3BA 5-minute orientation
- Skim a recent paper: Two Novel Functional Mutations in Promoter Region of SCN3B Gene Associated with Atrial FibrillationInfluential work since 2022
- Pick up a classic book: Strukturelle und kristallphysikalische Charakterisierung der komplexen Thiosulfate vom Typ Aā[B(SāOā)ā]XāThe most-reprinted book on the subject
- Read the landmark paper: Mutations in sodium channel Ī²-subunit SCN3B are associated with early-onset lone atrial fibrillationCited 112 times
- Go sideways: SCN2BA closely related topic
- Go sideways: SCN1BA closely related topic
š Definitions
No dictionary entry for this exact phrase.
šļø The subject at a glance
š Landmark papers (most cited)
Mutations in sodium channel Ī²-subunit SCN3B are associated with early-onset lone atrial fibrillation
The sodium channel -subunit SCN3b modulates the kinetics of SCN5a and is expressed heterogeneously in sheep heart
Is the voltage-gated sodium channel Ī²3 subunit (SCN3B) a biomarker for glioma?
Loss-of-function mutation of the SCN3B-encoded sodium channel 3 subunit associated with a case of idiopathic ventricular fibrillation
Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population
Novel <i>SCN3B</i> Mutation Associated With Brugada Syndrome Affects Intracellular Trafficking and Function of Nav1.5
Identification of SCN3B as a novel p53-inducible proapoptotic gene
Scn3b knockout mice exhibit abnormal ventricular electrophysiological properties
š Influential since 2022
Two Novel Functional Mutations in Promoter Region of SCN3B Gene Associated with Atrial Fibrillation
A novel SCN3B in-frame codon deletion in a Brugada syndrome patient: Implications for disrupted NaV1.5 function
Enterotoxinārelated genes PPFIA4 and SCN3B promote colorectal cancer development and progression
miR-190a-5p Partially Represses the Abnormal Electrical Activity of SCN3B in Cardiac Arrhythmias by Downregulation of IL-2
Identification of a novel Scn3b mutation in a Chinese Brugada syndrome pedigree: implications for Nav1.5 electrophysiological properties and intracellular distribution of Nav1.5 and NavĪ²3
š Books worth reading
- šStrukturelle und kristallphysikalische Charakterisierung der komplexen Thiosulfate vom Typ Aā[B(SāOā)ā]XāPeter Held Ā· 1994
Ranked by number of editions on Open Library, a rough measure of how lasting a book is.
š Related topics
- SCN2B Sodium channel subunit beta-2 is a protein that in humans is encoded by the SCN2B gene. Sodium channel GRCh38: Ensembl release 89: ENSG00000149575 ā Ensemblā¦
- SCN1B 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 generationā¦
- KCNAB3 Voltage-gated potassium channel subunit beta-3 is a protein that in humans is encoded by the KCNAB3 gene. The protein encoded by this gene is a voltage-gatedā¦
- CACNG1 Voltage-dependent calcium channel gamma-1 subunit is a protein that in humans is encoded by the CACNG1 gene. L-type calcium channels are composed of fiveā¦
- CACNB3 Voltage-dependent L-type calcium channel subunit beta-3 is a protein that in humans is encoded by the CACNB3 gene. Voltage-dependent calcium channel GRCh38:ā¦
- SCN4B Sodium channel Ī²-subunit 4, also known as SCN4B or NaĪ²4, is an auxiliary sodium channel subunit that can alter the kinetics of sodium channels. The proteinā¦
- KCNAB1 Voltage-gated potassium channel subunit beta-1 is a protein that in humans is encoded by the KCNAB1 gene. Potassium channels represent the most complexā¦
- CACNG4 Voltage-dependent calcium channel gamma-4 subunit is a protein that in humans is encoded by the CACNG4 gene. L-type calcium channels are composed of fiveā¦