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GENATLAS PHENOTYPE

last update : 13/07/2006

Symbol	JLNS2
Location	21q22.2
Name	Jervell-Lange-Nielsen 2
Corresponding gene	KCNE1
related resource	Long QT Syndrome Database
Main clinical features	cardioauditory syndrome of congenital neurosensory deafness with a long QT, syncopal attacks and a high risk of sudden death
Genetic determination	autosomal recessive
Function/system disorder	cardiovascular
	ear
Type	disease

Gene product

Name	potassium voltage-gated channel, Isk-related subfamily member 1 (KCNE1)