KCNE2

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

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Amber KCNE2 in Incidentalome


Version 0.301

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Long QT syndrome 6, MIM# 613693
Tags
  • cardiac

Amber KCNE2 in Long QT Syndrome


Level 2: Cardiovascular disorders
Version 0.61

Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Arrhythmia_SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Victorian Clinical Genetics Services
    Phenotypes
    • Long QT syndrome

    Amber KCNE2 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • BabySeq Category B gene
    Phenotypes
    • Long QT syndrome-6

    Amber KCNE2 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.114

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • BabySeq Category B gene
    • Expert Review Amber
    Phenotypes
    • Long QT syndrome-6