impaired left ventricular function Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0005162
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Genes

20 genes associated with the impaired left ventricular function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
NCAM1 neural cell adhesion molecule 1 1.29386
CERS6 ceramide synthase 6 1.10917
PKD1L3 polycystic kidney disease 1-like 3 1.07931
EXT1 exostosin glycosyltransferase 1 1.07253
NTRK2 neurotrophic tyrosine kinase, receptor, type 2 1.03374
ADAMTS14 ADAM metallopeptidase with thrombospondin type 1 motif, 14 1.00878
DLC1 DLC1 Rho GTPase activating protein 0.971375
CD36 CD36 molecule (thrombospondin receptor) 0.969142
PRKCE protein kinase C, epsilon 0.966714
FMN2 formin 2 0.951596
ABL2 ABL proto-oncogene 2, non-receptor tyrosine kinase 0.948539
EGFLAM EGF-like, fibronectin type III and laminin G domains 0.937598
WISP1 WNT1 inducible signaling pathway protein 1 0.909649
MORC1 MORC family CW-type zinc finger 1 0.894825
NRG1 neuregulin 1 0.890995
MTDH metadherin 0.890832
MEST mesoderm specific transcript 0.883466
LAMA1 laminin, alpha 1 0.871419
SCD5 stearoyl-CoA desaturase 5 0.871419
CLINT1 clathrin interactor 1 0.853555