cardiomyopathies Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. (Human Disease Ontology, DOID_0050700)
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10 genes associated with the disease cardiomyopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ACTC1 actin, alpha, cardiac muscle 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
KNG1 kininogen 1
MYBPC3 myosin binding protein C, cardiac
MYH7 myosin, heavy chain 7, cardiac muscle, beta
PLAT plasminogen activator, tissue
SLC22A5 solute carrier family 22 (organic cation/carnitine transporter), member 5
TNF tumor necrosis factor
TNNT2 troponin T type 2 (cardiac)