dilated cardiomyopathy Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An intrinsic cardiomyopathy that results in damage to the myocardium causing the heart to pump blood inefficiently.|A form of CARDIAC MUSCLE disease that is characterized by ventricular dilation, VENTRICULAR DYSFUNCTION, and HEART FAILURE. Risk factors include SMOKING; ALCOHOL DRINKING; HYPERTENSION; INFECTION; PREGNANCY; and mutations in the LMNA gene encoding LAMIN TYPE A, a NUCLEAR LAMINA protein.|decreased function of the heart associated with cardiac enlargement and congestive heart failure (Experimental Factor Ontology, EFO_0000407)
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Genes

8 genes associated with the disease dilated cardiomyopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CSRP3 cysteine and glycine-rich protein 3 (cardiac LIM protein)
DMD dystrophin
LMNA lamin A/C
MYH7 myosin, heavy chain 7, cardiac muscle, beta
PDLIM3 PDZ and LIM domain 3
SCN5A sodium channel, voltage gated, type V alpha subunit
TCAP titin-cap
TNNT2 troponin T type 2 (cardiac)