internal hemorrhage Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description The presence of hemorrhage within the body. (Human Phenotype Ontology, HP_0011029)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0011029
Similar Terms
Downloads & Tools

Genes

7 genes associated with the internal hemorrhage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
SLC39A11 solute carrier family 39, member 11 0.661809
ST6GALNAC3 ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 0.602436
TBC1D9 TBC1 domain family, member 9 (with GRAM domain) 0.58687
WWOX WW domain containing oxidoreductase 0.572823
MGAT5B mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, isozyme B 0.572823
NPAS3 neuronal PAS domain protein 3 0.522136
DPYSL2 dihydropyrimidinase-like 2 0.466578
Funding