Noncompaction Cardiomyopathy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A type of cardiomyopathy characterized anatomically by deep trabeculations in the ventricular wall, which define recesses communicating with the main ventricular chamber. (Human Phenotype Ontology, HP_0012817)
External Link https://www.disgenet.org/browser/0/1/0/C1839832
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Genes

15 genes associated with the disease Noncompaction Cardiomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
CSRP3 cysteine and glycine-rich protein 3 (cardiac LIM protein)
DES desmin
DNAJC19 DnaJ (Hsp40) homolog, subfamily C, member 19
DTNA dystrobrevin, alpha
HCN4 hyperpolarization activated cyclic nucleotide gated potassium channel 4
MYBPC3 myosin binding protein C, cardiac
MYH7 myosin, heavy chain 7, cardiac muscle, beta
NUMB numb homolog (Drosophila)
NUMBL numb homolog (Drosophila)-like
SDHA succinate dehydrogenase complex, subunit A, flavoprotein (Fp)
SDHAF1 succinate dehydrogenase complex assembly factor 1
SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
SDHD succinate dehydrogenase complex, subunit D, integral membrane protein
TTN titin