Gene: [21q22/KCNE1] potassium voltage-gated channel, Isk-related subfamily, member 1; minimal potassium ion channel (minK); Jervell and Lange-Nielsen syndrome (JLNS; MIM:220400); long QT syndrome (LQTS; LQT5); [IsK minK ]


REL

See FAM:KCN/00.0.

REF

LOC "Chevillard C &: Genomics, 15, N1, 243-245, 1993
MAP "Chumakov I &: Nature, 359, N6394, 380-387, 1992
MUT "Duggal P &: Circulation, 97, N2, 142-146, 1998
POL "Lai LP &: Gene, 151, N1-2, 339-340, 1994
LOC "Malo MS &: Gene, 159, N2, 273-275, 1995
PRO,LOC "McPherson &: CCG, 58, (HGM11), 1979, 1991
MUT "Schulze-Bahr E &: Nature Genet, 17, N3, 267-268, 1997
MUT "Tyson J &: Hum Mol Genet, 6, N12, 2179-2185, 1997

SWI

SWISSPROT: P15382

KEY

neu, mem, ion, sign

CLA

coding, basic

LOC

21 q22.1-.2

MIM

MIM: 176261

SYN

IsK minK

Смотрите также:

  • Удлинение интервала QT врожденное (LQTS)
  • KCNE1 (LQT5) ген
  • ген альфа-1 субъединицы калиевого канала типа L (CCHL1A2)
  • Ервел-Лангне-Нельсона синдром (JLNS)