Abruptio Placentae Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A placenta disease that is characterized by separation of the placental lining from the uterus of the mother. (Human Disease Ontology, DOID_9667)
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Genes

22 genes associated with the Abruptio Placentae phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
BHMT betaine--homocysteine S-methyltransferase
CTLA4 cytotoxic T-lymphocyte-associated protein 4
EPHX1 epoxide hydrolase 1, microsomal (xenobiotic)
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
FGB fibrinogen beta chain
HLA-A major histocompatibility complex, class I, A
HLA-B major histocompatibility complex, class I, B
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HLA-DRB3 major histocompatibility complex, class II, DR beta 3
HLA-DRB4 major histocompatibility complex, class II, DR beta 4
HLA-DRB5 major histocompatibility complex, class II, DR beta 5
IL1RN interleukin 1 receptor antagonist
MTHFD1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
NOS3 nitric oxide synthase 3 (endothelial cell)
RFC1 replication factor C (activator 1) 1, 145kDa
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
THBD thrombomodulin