Gene table: search width pubmed_id = 15761194


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Short QT syndrome 3 - (AD)
10.155
15761194
KCNJ2 (17q24.3)
Potassium channel, inwardly rectifying, dubfamily J, member 2
* Long QT syndrome-7 - LQT7
* Atrial fibrillation, 9 - ATFB9
* Andersen-Tawill syndrome cardiodysrythmic periodic paralysis
* Periodic paralysis, potassium-sensitive cardiodysrhythmic Andersen-Tawil syndrom - ATS