impaired platelet aggregation Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality in the rate and degree to which platelets aggregate after the addition of an agonist that stimulates platelet clumping. Platelet aggregation is measured using aggregometer to measure the optical density of platelet-rich plasma, whereby platelet aggregation causes the plasma to become more transparent. (Human Phenotype Ontology, HP_0003540)
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14 genes associated with the impaired platelet aggregation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
PEAR1 platelet endothelial aggregation receptor 1 1.9103
GLIS3 GLIS family zinc finger 3 1.38229
LDLRAD4 low density lipoprotein receptor class A domain containing 4 1.27804
MME membrane metallo-endopeptidase 1.25304
IPCEF1 interaction protein for cytohesin exchange factors 1 1.1725
LDHAL6A lactate dehydrogenase A-like 6A 1.16319
PCGF5 polycomb group ring finger 5 1.15702
ANKS1B ankyrin repeat and sterile alpha motif domain containing 1B 1.14999
ZNF583 zinc finger protein 583 1.14406
NEURL1 neuralized E3 ubiquitin protein ligase 1 1.12851
CASC15 cancer susceptibility candidate 15 (non-protein coding) 1.11876
MRVI1 murine retrovirus integration site 1 homolog 1.04365
SGCZ sarcoglycan, zeta 0.919744
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1 0.882984