Genomics England

BAG3

BCL2 associated athanogene 3

Panel	Mode of inheritance	Details
Filter panels5 panels
Green in Dilated and arrhythmogenic cardiomyopathy Component of the following Super Panels: - Sudden unexplained death or survivors of a cardiac event - Unexplained death in infancy and sudden unexplained death in childhood R-numbers: R132 Signed-off version 2.36	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Cardiomyopathy, dilated, 1HH, 613881, Myopathy, myofibrillar, 6, 612954
Green in Distal myopathies Component of the following Super Panels: - Hypotonic infant - Other rare neuromuscular disorders Signed-off version 6.3	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes myofibrillar myopathy 6, 612954
Green in Hereditary neuropathy or pain disorder R-numbers: R78 Signed-off version 6.163	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Phenotypes Myopathy, myofibrillar, 6 612954, Cardiomyopathy, dilated, 1HH, 613881
Green in Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies Component of the following Super Panels: - Hypotonic infant - Other rare neuromuscular disorders R-numbers: R82 Signed-off version 4.40	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Myopathy, myofibrillar, 6, 612954
Green in Paediatric or syndromic cardiomyopathy Component of the following Super Panels: - Unexplained death in infancy and sudden unexplained death in childhood R-numbers: R135 Signed-off version 6.7	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phenotypes Cardiomyopathy, dilated, 1HH