Gene and Protein Information
Species	TM	AA	Chromosomal Location	Gene Symbol	Gene Name	Reference
Human	-	569	7q36.1	PRKAG2	protein kinase AMP-activated non-catalytic subunit gamma 2
Mouse	-	566	5 A3	Prkag2	protein kinase, AMP-activated, gamma 2 non-catalytic subunit
Rat	-	326	4q11	Prkag2	protein kinase AMP-activated non-catalytic subunit gamma 2

Previous and Unofficial Names

protein kinase, AMP-activated, gamma 2 non-catalytic subunit | AMPK subunit gamma-2 | AAKG | AAKG2 | CMH6 | WPWS | protein kinase

Database Links
Alphafold	Q9UGJ0 (Hs), Q91WG5 (Mm)
ChEMBL Target	CHEMBL2453 (Hs)
Ensembl Gene	ENSG00000106617 (Hs), ENSMUSG00000028944 (Mm), ENSRNOG00000009085 (Rn)
Entrez Gene	51422 (Hs), 108099 (Mm), 373545 (Rn)
Human Protein Atlas	ENSG00000106617 (Hs)
KEGG Gene	hsa:51422 (Hs), mmu:108099 (Mm), rno:373545 (Rn)
OMIM	602743 (Hs)
Pharos	Q9UGJ0 (Hs)
RefSeq Nucleotide	NM_016203 (Hs), NM_001040633 (Hs), NM_024429 (Hs), NM_001170556 (Mm), NM_145401 (Mm), NM_001170555 (Mm), NM_184051 (Rn)
RefSeq Protein	NP_057287 (Hs), NP_001035723 (Hs), NP_077747 (Hs), NP_001164026 (Mm), NP_001164027 (Mm), NP_663376 (Mm), NP_908940 (Rn)
UniProtKB	Q9UGJ0 (Hs), Q91WG5 (Mm)
Wikipedia	PRKAG2 (Hs)

Clinically-Relevant Mutations and Pathophysiology
Disease:  Cardiomyopathy, familial hypertrophic 6; CMH6 Synonyms: Familial hypertrophic cardiomyopathy [Disease Ontology: DOID:11986] Familial isolated hypertrophic cardiomyopathy [Orphanet: ORPHA155] Disease Ontology: DOID:11986 OMIM: 600858 Orphanet: ORPHA155
Disease:  Glycogen storage disease of heart, lethal congenital OMIM: 261740
Disease:  Wolff-Parkinson-White syndrome Disease Ontology: DOID:384 OMIM: 194200 Orphanet: ORPHA907