Gene table: search width pubmed_id = 11371514


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

protein
All allelic disease phenotypes - locus/disease symbols
Familial hypertrophic cardiomyopathy, 6 - (AD)
10.5
11371514
PRKAG2 (7q31)
Protein kinase, AMP-activated, gamma 2 non-catalytic subunit
* Cardiomyopathy, familial hypertrophic, with Wolff-Parkinson-white syndrome - CMH6
* glycogen storage disease of heart, lethal congenital