Placenta Diseases Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

19 genes associated with the Placenta Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ADRB2 adrenoceptor beta 2, surface
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
ANGPT1 angiopoietin 1
CHST11 carbohydrate (chondroitin 4) sulfotransferase 11
CHST12 carbohydrate (chondroitin 4) sulfotransferase 12
CHST13 carbohydrate (chondroitin 4) sulfotransferase 13
CPB2 carboxypeptidase B2 (plasma)
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
FCGR2A Fc fragment of IgG, low affinity IIa, receptor (CD32)
FLT1 fms-related tyrosine kinase 1
IL1RAP interleukin 1 receptor accessory protein
IL4 interleukin 4
MBL2 mannose-binding lectin (protein C) 2, soluble
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
PLAT plasminogen activator, tissue
PLAUR plasminogen activator, urokinase receptor
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1