Symbol Name ID |
Prkag2
protein kinase, AMP-activated, gamma 2 non-catalytic subunit MGI:1336153 |
Darker colors indicate more annotations |
Human Phenotypes | Biventricular hypertrophy |
Cardiomyopathy |
Hypertrophic cardiomyopathy |
Asymmetric septal hypertrophy |
Increased myocardial glycogen content |
Myofiber disarray |
Pericardial effusion |
Cardiomegaly |
Hypotension |
Shortened PR interval |
Prolonged QRS complex |
ST segment depression |
ST segment elevation |
T-wave inversion |
Left axis deviation |
Sinus bradycardia |
Bradycardia |
Aborted sudden cardiac death |
Sudden cardiac death |
Palpitations |
Atrial fibrillation |
Paroxysmal atrial fibrillation |
Atrial flutter |
Ventricular fibrillation |
Ventricular preexcitation |
Ventricular preexcitation with multiple accessory pathways |
Wolff-Parkinson-White syndrome |
Atrioventricular block |
Left bundle branch block |
Congestive heart failure |
Syncope |
Disease(s) Associated with PRKAG2 | |||||||||||||||||||||||||||||||
hypertrophic cardiomyopathy 6 | |||||||||||||||||||||||||||||||
lethal congenital glycogen storage disease of heart | |||||||||||||||||||||||||||||||
Wolff-Parkinson-White syndrome |
Mouse Phenotypes | increased cardiac muscle glycogen level |
abnormal sinoatrial node morphology |
decreased cardiac muscle contractility |
decreased heart rate |
sinus bradycardia |
increased heart rate |
abnormal sinoatrial node conduction |
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Availability | Mouse Genotype | |||||||
Prkag2tm1.1Geno/Prkag2tm1.1Geno | ||||||||
Prkag2tm1.1Geno/Prkag2tm1.1Geno Edil3Tg(Sox2-cre)1Amc/Edil3+ (conditional) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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