abnormality of the pleura Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the pulmonary pleura, the thin, transparent membrane which covers the lungs and lines the inside of the chest walls. (Human Phenotype Ontology, HP_0002103)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0002103
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Genes

9 genes associated with the abnormality of the pleura phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
PVT1 Pvt1 oncogene (non-protein coding) 1.01655
SLC7A14 solute carrier family 7, member 14 0.949798
THRB thyroid hormone receptor, beta 0.872838
PLGRKT plasminogen receptor, C-terminal lysine transmembrane protein 0.861268
MMP14 matrix metallopeptidase 14 (membrane-inserted) 0.831588
CEP350 centrosomal protein 350kDa 0.803642
ADAMTS2 ADAM metallopeptidase with thrombospondin type 1 motif, 2 0.776638
ETV1 ets variant 1 0.74676
SHC4 SHC (Src homology 2 domain containing) family, member 4 0.696351