pulmonary embolism Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An artery disease characterized by a blockage of the main artery of the lung or one of its branches by a substance that has travelled from elsewhere in the body, e.g. a blood clot. (Human Disease Ontology, DOID_9477)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0002204
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Genes

18 genes associated with the pulmonary embolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
AK4 adenylate kinase 4 1.38847
ZC3H3 zinc finger CCCH-type containing 3 1.37994
YEATS4 YEATS domain containing 4 1.35521
ARHGEF28 Rho guanine nucleotide exchange factor (GEF) 28 1.32793
EFEMP1 EGF containing fibulin-like extracellular matrix protein 1 1.32793
PLXNA4 plexin A4 1.32793
FAM228A family with sequence similarity 228, member A 1.32793
CHRM3 cholinergic receptor, muscarinic 3 1.30781
DLC1 DLC1 Rho GTPase activating protein 1.30781
PCMTD1 protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1 1.29386
PAPPA2 pappalysin 2 1.29386
SMIM23 small integral membrane protein 23 1.29386
WDR63 WD repeat domain 63 1.28282
FGF14 fibroblast growth factor 14 1.28282
MGLL monoglyceride lipase 1.26545
FBXO15 F-box protein 15 1.26545
RSAD2 radical S-adenosyl methionine domain containing 2 1.25251
NAALADL2 N-acetylated alpha-linked acidic dipeptidase-like 2 1.25251