KCNE2

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

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Red KCNE2 in Incidentalome


Version 0.433

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

Red KCNE2 in Long QT Syndrome


Level 2: Cardiovascular disorders
Version 0.63

Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Arrhythmia_SuperPanel
  • 2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Long QT syndrome
    Tags
    • disputed

    Red KCNE2 in Mendeliome


    Version 1.4782

    2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Red
    • Expert Review Red
    Phenotypes
    • Long QT syndrome
    Tags
    • disputed

    Amber KCNE2 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.280

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

    Red KCNE2 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.148

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • BabySeq Category B gene
    Phenotypes
    • Long QT syndrome 6, MIM# 613693