KCNJ2

potassium voltage-gated channel subfamily J member 2
OMIM: 600681
PanelMode of inheritanceDetails
5 panels
Green
in Clefting
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS, Cleft palate
R-numbers: R21
Signed-off version 1.92
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Andersen syndrome 170390
Component of the following Super Panels:
  • - Cardiac arrhythmias
  • - Sudden cardiac death
R-numbers: R127
Signed-off version 2.20
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Andersen syndrome (170390), Atrial fibrillation, familial, 9 (613980), ANDERSEN SYNDROME (170390), LONG QT SYNDROME 7 (170390), Short QT syndrome 3 (609622)
Component of the following Super Panels:
  • - Cardiac arrhythmias
  • - Sudden cardiac death
R-numbers: R130
Signed-off version 2.4
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Atrial fibrillation, familial, 9 (613980), Short QT syndrome 3 609622, Short QT syndrome 3 (609622), Andersen syndrome (170390), ventricular tacyarrhythmia, short qt, atrial fibrillation
R-numbers: R76
Signed-off version 1.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Andersen syndrome, 170390