KCNE2

potassium voltage-gated channel subfamily E regulatory subunit 2
OMIM: 603796, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red KCNE2 in Short QT syndrome


Version 3.10
Latest signed off version: v3.1 (22 Mar 2023)

Component of the following Super Panels:

  • Cardiac arrhythmias
  • Sudden unexplained death or survivors of a cardiac event
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • North West GLH
    • Emory Genetics Laboratory
    • Long QT syndrome (Version 1.5)
    Phenotypes
    • Long QT syndrome-6 (613693)
    • Atrial fibrillation, familial, 4 (611493)
    Amber KCNE2 in Long QT syndrome

    Level 3: Cardiac arrhythmia
    Level 2: Cardiovascular disorders
    Version 3.7
    Latest signed off version: v3.1 (22 Mar 2023)

    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, NOT imprinted
    Sources
    • Expert Review Amber
    • South West GLH
    • London South GLH
    • North West GLH
    • Emory Genetics Laboratory
    • Expert list
    • UKGTN
    • Illumina TruGenome Clinical Sequencing Services
    • Radboud University Medical Center, Nijmegen
    Phenotypes
    • Long QT syndrome 6 (613693)
    • Atrial fibrillation, familial, 4 (611493)