KCNE3

potassium voltage-gated channel subfamily E regulatory subunit 3
OMIM: 604433, Gene2Phenotype

4 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Red KCNE3 in Familial Meniere Disease Level 3: Other hearing and ear disorders Level 2: Hearing and ear disorders Version 1.4	review	Not set	Sources Literature
Red KCNE3 in Short QT syndrome Level 2: Cardiology Version 3.16 Latest signed off version: v3.14 (30 Apr 2025) Component of the following Super Panels: Cardiac arrhythmias Sudden unexplained death or survivors of a cardiac event Unexplained death in infancy and sudden unexplained death in childhood	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources North West GLH Brugada syndrome (Version 1.7) Long QT syndrome (Version 1.5) Phenotypes ?Brugada syndrome 6 (613119)
Red KCNE3 in Long QT syndrome Level 2: Cardiology Version 3.12 Latest signed off version: v3.10 (30 Apr 2025) Component of the following Super Panels: Cardiac arrhythmias Sudden unexplained death or survivors of a cardiac event Unexplained death in infancy and sudden unexplained death in childhood	review	Unknown	Sources South West GLH Literature Phenotypes Long QT syndrome Brugada syndrome
Red KCNE3 in Brugada syndrome and cardiac sodium channel disease Level 2: Cardiology Version 3.14 Latest signed off version: v3.12 (30 Apr 2025) Component of the following Super Panels: Cardiac arrhythmias Sudden unexplained death or survivors of a cardiac event Unexplained death in infancy and sudden unexplained death in childhood	review	Unknown	Sources Expert Review Red South West GLH London South GLH North West GLH Expert list Emory Genetics Laboratory Radboud University Medical Center, Nijmegen UKGTN Illumina TruGenome Clinical Sequencing Services Phenotypes ?Brugada syndrome 6, OMIM:613119