Gene table: search width pubmed_id = 20560207


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

protein
All allelic disease phenotypes - locus/disease symbols
Long QT syndrome 13 - (AD)
10.148
20560207
KCNJ5 (11 q24.3)
Potassium inwardly-rectifying channel, subfamily J, member 5
* Long QT syndrome 13 - LQT13
* Andersen-Tawill syndrome cardiodysrythmic periodic paralysis