cardiomyopathy Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A heart disease and a myopathy that is characterized by deterioration of the function of the heart muscle. (Human Disease Ontology, DOID_0050700)
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21 genes associated with the disease cardiomyopathy in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PHACTR1 phosphatase and actin regulator 1 1.45255
BAG3 BCL2-associated athanogene 3 0.850113
CELSR2 cadherin, EGF LAG seven-pass G-type receptor 2 0.825265
MRPS6 mitochondrial ribosomal protein S6 0.745324
ZBTB17 zinc finger and BTB domain containing 17 0.63207
MIA3 melanoma inhibitory activity family, member 3 0.63207
SMARCA4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 0.602429
CXCL12 chemokine (C-X-C motif) ligand 12 0.544585
WDR12 WD repeat domain 12 0.52461
C12ORF42 chromosome 12 open reading frame 42 0.403461
MARC1 mitochondrial amidoxime reducing component 1 0.345945
RCSD1 RCSD domain containing 1 0.311576
SLC22A3 solute carrier family 22 (organic cation transporter), member 3 0.297866
COL4A2 collagen, type IV, alpha 2 0.264872
CLEC14A C-type lectin domain family 14, member A 0.264872
PPP4R2 protein phosphatase 4, regulatory subunit 2 0.197766
TENM1 teneurin transmembrane protein 1 0.197766
LZTS1 leucine zipper, putative tumor suppressor 1 0.15771
LTA lymphotoxin alpha 0.15771
SETBP1 SET binding protein 1 0.126165
ADAMTS7 ADAM metallopeptidase with thrombospondin type 1 motif, 7 0.064973