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 |
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