dilated cardiomyopathy Gene Set

Dataset DISEASES Curated Gene-Disease Assocation 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 and characterized by an enlarged heart. (Human Disease Ontology, DOID_12930)
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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
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