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Short QT syndrome 2; SQT2

Disease ID:854
Name:Short QT syndrome 2; SQT2
Associated with:1 target
Synonyms
Familial short QT syndrome
Database Links
OMIM: 609621
Orphanet: ORPHA51083

Targets

Kv7.1
Role:  Gain of function mutations in KCNQ1 shortens action potentials, leading to shortened QT interval, sinus bradycardia and cardiac arrhythmia
References:  1,3
Mutations:  Kv7.1 is associated with 3 mutation. Click here for details

Ligands

No ligand related data available for Short QT syndrome 2; SQT2

References

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1. Bellocq C, van Ginneken AC, Bezzina CR, Alders M, Escande D, Mannens MM, BarĂ³ I, Wilde AA. (2004) Mutation in the KCNQ1 gene leading to the short QT-interval syndrome. Circulation, 109 (20): 2394-7. [PMID:15159330]

2. Chen YH, Xu SJ, Bendahhou S, Wang XL, Wang Y, Xu WY, Jin HW, Sun H, Su XY, Zhuang QN et al.. (2003) KCNQ1 gain-of-function mutation in familial atrial fibrillation. Science, 299 (5604): 251-4. [PMID:12522251]

3. Hong K, Piper DR, Diaz-Valdecantos A, Brugada J, Oliva A, Burashnikov E, Santos-de-Soto J, Grueso-Montero J, Diaz-Enfante E, Brugada P et al.. (2005) De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero. Cardiovasc Res, 68 (3): 433-40. [PMID:16109388]