Cardiomyopathy, Hypertrophic, Familial Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

23 genes associated with the Cardiomyopathy, Hypertrophic, Familial phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ACTC1 actin, alpha, cardiac muscle 1
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1 angiotensin II receptor, type 1
CALM3 calmodulin 3 (phosphorylase kinase, delta)
CMA1 chymase 1, mast cell
CRYAB crystallin, alpha B
CSRP3 cysteine and glycine-rich protein 3 (cardiac LIM protein)
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
DES desmin
GLA galactosidase, alpha
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
MYOZ2 myozenin 2
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit
SGCD sarcoglycan, delta (35kDa dystrophin-associated glycoprotein)
TNNC1 troponin C type 1 (slow)
TNNI3 troponin I type 3 (cardiac)
TNNT2 troponin T type 2 (cardiac)
TPM1 tropomyosin 1 (alpha)
TTN titin