PRKAG2

protein kinase AMP-activated non-catalytic subunit gamma 2
OMIM: 602743, Gene2Phenotype

12 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 12 panels
Green PRKAG2 in Glycogen Storage Diseases Level 2: Metabolic disorders Version 1.3 Component of the following Super Panels: Metabolic Disorders Superpanel Progressive Neurological Conditions	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Glycogen storage disease of heart, lethal congenital, MIM# 261740
Green PRKAG2 in Hypertrophic cardiomyopathy_HCM Level 2: Cardiovascular disorders Version 1.10 Component of the following Super Panels: Adult Cardiac SuperPanel Cardiomyopathy_Adult_SuperPanel	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cardiomyopathy, hypertrophic 6, MIM# 600858
Green PRKAG2 in Incidentalome Version 0.360	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes Cardiomyopathy, hypertrophic 6, MIM# 600858 Glycogen storage disease of heart, lethal congenital, MIM# 261740 Tags cardiac
Green PRKAG2 in Additional findings_Adult Level 2: Screening Version 1.130	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Melbourne Genomics Health Alliance Phenotypes Cardiomyopathy, hypertrophic 6, MIM# 600858
Green PRKAG2 in Rhabdomyolysis and Metabolic Myopathy Level 2: Neurology and neurodevelopmental disorders Version 1.26 Component of the following Super Panels: Myopathy Superpanel Neuromuscular Superpanel Progressive Neurological Conditions	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Wolff-Parkinson-White syndrome 194200 Cardiomyopathy, hypertrophic 6 600858 Glycogen storage disease of heart, lethal congenital 261740
Green PRKAG2 in Cardiomyopathy_Paediatric Level 2: Cardiovascular disorders Version 0.207	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Green NHS GMS London South GLHSouth West GLH Victorian Clinical Genetics Services Phenotypes Cardiomyopathy, familial hypertrophic 6, Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome syndromic HCM
Red PRKAG2 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red BabySeq Category C gene BabySeq Category B gene BabySeq Category A gene Phenotypes Glycogen storage disease of heart, lethal congenital Wolff-Parkinson-White syndrome Cardiomyopathy, hypertrophic
Green PRKAG2 in Incidentalome_PREGEN_DRAFT Version 0.43	0 reviews	Unknown	Sources NSW Health Pathology Expert Review Green
Green PRKAG2 in Fetal anomalies Version 1.465	1 review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Genomics England PanelApp Phenotypes Glycogen storage disease of heart, lethal congenital, OMIM:261740 Lethal congenital glycogen storage disease of heart, MONDO:0009867
Red PRKAG2 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category C gene BabySeq Category A gene Expert Review Red BabySeq Category B gene Phenotypes Cardiomyopathy, hypertrophic Wolff-Parkinson-White syndrome Glycogen storage disease of heart, lethal congenital
Green PRKAG2 in Transplant Co-Morbidity Level 2: Screening Version 0.20	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Cardiomyopathy, hypertrophic 6, MIM# 600858
Green PRKAG2 in Cardiac conduction disease Level 2: Cardiovascular disorders Version 1.3 Component of the following Super Panels: Adult Cardiac SuperPanel Arrhythmia_SuperPanel	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green NHS GMS Phenotypes PRKAG2-related cardiomyopathy MONDO:0800484