Gene: [11p155/KCNQ1] potassium voltage-gated channel, KQT-like subfamily, member 1; potassium voltage-gated channel, shaker-related subfamily, member 9; potassium voltage-gated channel, shaker-related subfamily, member 8; long (electrocardiographic) QT syndrome 1, Ward-Romano syndrome; [KCNA9 KCNA8 ]
|
CAG |
There are four genetic forms of the long QT syndrome: LQT1, LQT2 (GEM:07q3/LQT2), LQT3 (GEM:03p21/SCN5A), and LQT4 (GEM:04q2/LQT4)." |
|
REL |
GEM:20q133/KCNQ2; GEM:08q24/KCNQ3. |
|
REF |
HET "Curran M &: J Clin Invest, 92, 799-803, 1993 HET,LIN,LOC "Jiang C &: Nature Genet, 8, 141-147, 1994 LIN,LOC,HET "Kainulainen K &: Hum Genet, 96, N4, 395-400, 1995 LIN,LOC "Keating M &: AJHG, 49, 1335-1339, 1991a LIN,LOC "Keating M &: Science, 252, 704-706, 1991b HET "Kerem B &: AJHG, 51, (Suppl), A192, 1992 HET "Ohzeki T &: J Int Med, 234, 227-229, 1993 LIN,LOC "Roy N &: Nature Genet, 8, N2, 113-114, 1994 LIN,LOC "Russell M &: AJHG, 57, N2, 503-507, 1995 HET "Tanaka T &: Hum Genet, 94, 380-384, 1994 CLO,SEQ,MUT "Wang Q &: Nature Genet, 12, 17-23, 1996 |
|
KEY |
neu, mem, ion, sign, card |
|
CLA |
coding, basic |
|
LOC |
11 p15.5 |
|
MIM |
MIM: 192500 |
|
SYN |
KCNA9 KCNA8 |
