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GENATLAS PHENOTYPE

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

Remark(s)