Disease phenotype
OMIM
Gene symbol (chromosome)
protein
protein
KCNE1 (21q22.1-q22.2)
potassium voltage-gated channel, Isk-related family, member 1
KCNQ1 (11p15.5)
potassium voltage-gated channel, KQT-like subfamily, member 1
Disease phenotype | OMIM | Gene symbol (chromosome) protein |
| Jervell and Lange-Nielsen syndrome | KCNE1 (21q22.1-q22.2) potassium voltage-gated channel, Isk-related family, member 1
| |
| jervell and lange-nielsen syndrome | KCNQ1 (11p15.5) potassium voltage-gated channel, KQT-like subfamily, member 1
|