dilated cardiomyopathy Gene Set

Dataset GWASdb SNP-Disease Associations
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)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:12930
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Genes

12 genes associated with the disease dilated cardiomyopathy in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
HSPB7 heat shock 27kDa protein family, member 7 (cardiovascular) 1.70767
BAG3 BCL2-associated athanogene 3 1.6622
ZBTB17 zinc finger and BTB domain containing 17 1.50906
HCG22 HLA complex group 22 1.35253
AKAP13 A kinase (PRKA) anchor protein 13 1.30031
RUNX1 runt-related transcription factor 1 1.29761
ADD2 adducin 2 (beta) 1.28797
DHX16 DEAH (Asp-Glu-Ala-His) box polypeptide 16 1.23283
RPS6KA1 ribosomal protein S6 kinase, 90kDa, polypeptide 1 1.16574
VWC2L von Willebrand factor C domain containing protein 2-like 0.837296
LOC100507462 uncharacterized LOC100507462 0.427749
SIPA1L1 signal-induced proliferation-associated 1 like 1 0.423102