dilated cardiomyopathy Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description An intrinsic cardiomyopathy that results in damage to the myocardium causing the heart to pump blood inefficiently.|A form of CARDIAC MUSCLE disease that is characterized by ventricular dilation, VENTRICULAR DYSFUNCTION, and HEART FAILURE. Risk factors include SMOKING; ALCOHOL DRINKING; HYPERTENSION; INFECTION; PREGNANCY; and mutations in the LMNA gene encoding LAMIN TYPE A, a NUCLEAR LAMINA protein.|decreased function of the heart associated with cardiac enlargement and congestive heart failure (Experimental Factor Ontology, EFO_0000407)
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Genes

33 genes involed in the disease dilated cardiomyopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ABCC9 ATP-binding cassette, sub-family C (CFTR/MRP), member 9
ACTC1 actin, alpha, cardiac muscle 1
ACTN2 actinin, alpha 2
ANKRD1 ankyrin repeat domain 1 (cardiac muscle)
BAG3 BCL2-associated athanogene 3
CRYAB crystallin, alpha B
CSRP3 cysteine and glycine-rich protein 3 (cardiac LIM protein)
DES desmin
DMD dystrophin
DSG2 desmoglein 2
EYA4 EYA transcriptional coactivator and phosphatase 4
LAMA4 laminin, alpha 4
LDB3 LIM domain binding 3
LMNA lamin A/C
MYBPC3 myosin binding protein C, cardiac
MYH6 myosin, heavy chain 6, cardiac muscle, alpha
MYH7 myosin, heavy chain 7, cardiac muscle, beta
MYPN myopalladin
PLN phospholamban
PSEN1 presenilin 1
PSEN2 presenilin 2
RBM20 RNA binding motif protein 20
SCN5A sodium channel, voltage gated, type V alpha subunit
SGCD sarcoglycan, delta (35kDa dystrophin-associated glycoprotein)
TAZ tafazzin
TCAP titin-cap
TMPO thymopoietin
TNNC1 troponin C type 1 (slow)
TNNI3 troponin I type 3 (cardiac)
TNNT2 troponin T type 2 (cardiac)
TPM1 tropomyosin 1 (alpha)
TTN titin
VCL vinculin