cardiomyopathies Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
Description A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS).|A disease of the heart muscle or myocardium proper. Cardiomyopathies may be classified as either primary or secondary, on the basis of etiology, or on the pathophysiology of the lesion: hypertrophic, dilated, or restrictive. (Experimental Factor Ontology, EFO_0000318)
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Genes

27 genes co-occuring with the biological term cardiomyopathies in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ATP2A2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
CD34 CD34 molecule
CXCL8 chemokine (C-X-C motif) ligand 8
DES desmin
DMD dystrophin
ENPEP glutamyl aminopeptidase (aminopeptidase A)
GJA1 gap junction protein, alpha 1, 43kDa
GSTM1 glutathione S-transferase mu 1
IL10 interleukin 10
LMNA lamin A/C
MAP3K5 mitogen-activated protein kinase kinase kinase 5
MYBPC3 myosin binding protein C, cardiac
MYH7 myosin, heavy chain 7, cardiac muscle, beta
MYPN myopalladin
NPPA natriuretic peptide A
PARK7 parkinson protein 7
PDLIM3 PDZ and LIM domain 3
PEPD peptidase D
PLN phospholamban
PTEN phosphatase and tensin homolog
RYR2 ryanodine receptor 2 (cardiac)
TNNC1 troponin C type 1 (slow)
TNNI3 troponin I type 3 (cardiac)
TTN titin
TXN thioredoxin
YWHAE tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, epsilon