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  3. SCN4B
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Sudden death in young people

Gene: SCN4B

No list
SCN4B (sodium voltage-gated channel beta subunit 4)
EnsemblGeneIds (GRCh38): ENSG00000177098
EnsemblGeneIds (GRCh37): ENSG00000177098
OMIM: 608256, Gene2Phenotype
SCN4B is in 3 panels

1 review

Rebecca Foulger (Genomics England curator)

Comment on list classification: Changed rating from red to grey: SCN4B is red on the V1.0 Long QT syndrome panel.
Created: 6 Dec 2016, 4:34 p.m.
Created: 6 Dec 2016, 4:34 p.m.

Panel version: 0.22

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Removed
  • UKGTN
Phenotypes
  • Molecular autopsy
  • Arrhythmia/Cardiac Arrest
  • Long QT syndrome
Tags
curated_removed
OMIM
608256
Clinvar variants
Variants in SCN4B
Penetrance
Complete
Panels with this gene

History Filter Activity

26 Feb 2021, Gel status: 0

Added Tag

Arina Puzriakova (Genomics England Curator)

Tag curated_removed tag was added to gene: SCN4B.

19 Dec 2016, Gel status: 0

panel promoted to version 1

Ellen Thomas (Genomics England Curator)

This panel contains genes which aren't arrhythmic or metabolic causes of sudden death with normal post mortem.

6 Dec 2016, Gel status: 0

Gene classified by Genomics England curator

Rebecca Foulger (Genomics England curator)

This gene has been removed from the panel.

6 Dec 2016, Gel status: 1

Added New Source

Rebecca Foulger (Genomics England curator)

SCN4B was added to Sudden death in young peoplepanel. Sources: UKGTN

6 Dec 2016, Gel status: 0

Created

Rebecca Foulger (Genomics England curator)

SCN4B was created by rfoulger