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Hypertrophic cardiomyopathy_HCM v1.3 POPDC2 Chirag Patel Classified gene: POPDC2 as Amber List (moderate evidence)
Hypertrophic cardiomyopathy_HCM v1.3 POPDC2 Chirag Patel Gene: popdc2 has been classified as Amber List (Moderate Evidence).
Hypertrophic cardiomyopathy_HCM v1.3 POPDC2 Chirag Patel Classified gene: POPDC2 as Amber List (moderate evidence)
Hypertrophic cardiomyopathy_HCM v1.3 POPDC2 Chirag Patel Gene: popdc2 has been classified as Amber List (Moderate Evidence).
Hypertrophic cardiomyopathy_HCM v1.3 POPDC2 Chirag Patel Classified gene: POPDC2 as Amber List (moderate evidence)
Hypertrophic cardiomyopathy_HCM v1.3 POPDC2 Chirag Patel Gene: popdc2 has been classified as Amber List (Moderate Evidence).
Hypertrophic cardiomyopathy_HCM v1.3 POPDC2 Chirag Patel Classified gene: POPDC2 as Amber List (moderate evidence)
Hypertrophic cardiomyopathy_HCM v1.3 POPDC2 Chirag Patel Gene: popdc2 has been classified as Amber List (Moderate Evidence).
Hypertrophic cardiomyopathy_HCM v1.2 POPDC2 Chirag Patel Classified gene: POPDC2 as Amber List (moderate evidence)
Hypertrophic cardiomyopathy_HCM v1.2 POPDC2 Chirag Patel Gene: popdc2 has been classified as Amber List (Moderate Evidence).
Hypertrophic cardiomyopathy_HCM v1.2 POPDC2 Chirag Patel Classified gene: POPDC2 as Amber List (moderate evidence)
Hypertrophic cardiomyopathy_HCM v1.2 POPDC2 Chirag Patel Gene: popdc2 has been classified as Amber List (Moderate Evidence).
Hypertrophic cardiomyopathy_HCM v1.1 POPDC2 Chirag Patel gene: POPDC2 was added
gene: POPDC2 was added to Hypertrophic cardiomyopathy_HCM. Sources: Literature
Mode of inheritance for gene: POPDC2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: POPDC2 were set to PMID: 40409267
Phenotypes for gene: POPDC2 were set to Hypertrophic cardiomyopathy MONDO:0005045, POPDC2-related
Review for gene: POPDC2 was set to AMBER
Added comment: 6 individuals from 4 families with biallelic variants in POPDC2 and sinus node dysfunction (4/6), AV conduction defects (6/6), and hypertrophic cardiomyopathy (2/6). The variants (2 missense, 2 truncating, 1 indel) are predicted to diminish the ability of POPDC2 to bind cAMP. Muscle biopsy of an affected individual did not show clear myopathic disease. None of the familial variants were associated with clinical outcomes in heterozygous state, (using population-level genetic data of > 1 million individuals).
Sources: Literature