Disease table



Disease phenotype
OMIM
Gene symbol (chromosome)
protein
jervell and lange-nielsen syndrome (10.118, 10.102, 7.17, 7.16, 10.122, 10.116)
220400
KCNQ1 (11p15.5)
Potassium voltage-gated channel, KQT-like subfamily, member 1



Jervell and Lange-Nielsen syndrome (10.106, 7.19)
220400
KCNE1 (21q22.1-q22.2)
Potassium voltage-gated channel, Isk-related family, member 1