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References OMIM Gene GeneReviews HGMD HGNC
last update : 22-04-2010
Symbol LQT6
Location 21q22.11
Name long QT syndrome with ventricular tachyarrhythmia, type 6
Corresponding gene KCNE2
Main clinical features
  • predisposing to torsades de pointes and ventricular fibrillation,associated to diminishing potassium currents (see genes KCNE2, KCNQ1)
  • Genetic determination autosomal dominant
    Related entries auditory stimulus-induced arrhythmia
    Function/system disorder cardiovascular
    Type disease
    Gene product
    Name potassium voltage-gated channel KCNE2