hypertrophic cardiomyopathy Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An intrinsic cardiomyopathy that is characterized by abnormal thickening (hypertrophy) of the heart without any obvious cause. (Human Disease Ontology, DOID_11984)
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Genes

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

Symbol Name
ACTC1 actin, alpha, cardiac muscle 1
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
DES desmin
HLA-B major histocompatibility complex, class I, B
MYBPC3 myosin binding protein C, cardiac
MYH7 myosin, heavy chain 7, cardiac muscle, beta
MYL2 myosin, light chain 2, regulatory, cardiac, slow
MYL3 myosin, light chain 3, alkali; ventricular, skeletal, slow
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit
TNNC1 troponin C type 1 (slow)
TNNI3 troponin I type 3 (cardiac)
TNNT2 troponin T type 2 (cardiac)
TPM1 tropomyosin 1 (alpha)