Asymmetric Septal Hypertrophy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Hypertrophic cardiomyopathy with an asymmetrical pattern of hypertrophy, with a predilection for the interventricular septum and myocyte disarray. (Human Phenotype Ontology, HP_0001670)
External Link https://www.disgenet.org/browser/0/1/0/C0205700
Similar Terms
Downloads & Tools

Genes

31 genes associated with the disease Asymmetric Septal Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADRA2A adrenoceptor alpha 2A
BDNF brain-derived neurotrophic factor
CAV3 caveolin 3
CD36 CD36 molecule (thrombospondin receptor)
CIDEC cell death-inducing DFFA-like effector c
EPCAM epithelial cell adhesion molecule
GNAI1 guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 1
GNS glucosamine (N-acetyl)-6-sulfatase
GSTP1 glutathione S-transferase pi 1
HGSNAT heparan-alpha-glucosaminide N-acetyltransferase
HMGB1 high mobility group box 1
IL37 interleukin 37
MTOR mechanistic target of rapamycin (serine/threonine kinase)
MYBPC3 myosin binding protein C, cardiac
MYD88 myeloid differentiation primary response 88
MYH6 myosin, heavy chain 6, cardiac muscle, alpha
MYH7 myosin, heavy chain 7, cardiac muscle, beta
MYL2 myosin, light chain 2, regulatory, cardiac, slow
MYLK2 myosin light chain kinase 2
NAGLU N-acetylglucosaminidase, alpha
NLRC4 NLR family, CARD domain containing 4
NOXO1 NADPH oxidase organizer 1
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
PNPLA3 patatin-like phospholipase domain containing 3
PPARD peroxisome proliferator-activated receptor delta
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit
RASSF1 Ras association (RalGDS/AF-6) domain family member 1
SGSH N-sulfoglucosamine sulfohydrolase
TACSTD2 tumor-associated calcium signal transducer 2
TLR4 toll-like receptor 4
UBD ubiquitin D