PRKAG2

Summary

PRKAG2 is a gene^[1]. PRKAG2 ranks in the top 2% of gene entities by monthly Wikipedia readership (14 views/month).^[2]

Key Facts

• PRKAG2's instance of is recorded as gene^[3].
• PRKAG2 is a type of protein-coding gene^[4].
• PRKAG2's HomoloGene ID is recorded as 136125^[5].
• PRKAG2's genomic start is recorded as 151253197^[6].
• PRKAG2's genomic start is recorded as 151556124^[7].
• PRKAG2's genomic end is recorded as 151877125^[8].
• PRKAG2's genomic end is recorded as 151574210^[9].
• PRKAG2's ortholog is recorded as Prkag2^[10].
• PRKAG2's ortholog is recorded as Prkag2^[11].
• PRKAG2's ortholog is recorded as prkag2b^[12].
• PRKAG2's encodes is recorded as Protein kinase AMP-activated non-catalytic subunit gamma 2^[13].
• PRKAG2's found in taxon is recorded as Homo sapiens^[14].
• PRKAG2's chromosome is recorded as human chromosome 7^[15].
• PRKAG2's genetic association is recorded as bipolar disorder^[16].
• PRKAG2's genetic association is recorded as kidney disease^[17].
• PRKAG2's genetic association is recorded as Wolff–Parkinson–White syndrome^[18].
• PRKAG2's genetic association is recorded as hypertrophic cardiomyopathy 6^[19].
• PRKAG2's genetic association is recorded as lethal congenital glycogen storage disease of heart^[20].

Why It Matters

PRKAG2 ranks in the top 2% of gene entities by monthly Wikipedia readership (14 views/month).^[2]