Antithrombin III Deficiency Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An inherited blood coagulation disease characterized by the tendency to form clots in the veins. (Human Disease Ontology, DOID_3755)
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Genes

6 genes associated with the Antithrombin III Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
PROC protein C (inactivator of coagulation factors Va and VIIIa)
PROS1 protein S (alpha)
SERPINC1 serpin peptidase inhibitor, clade C (antithrombin), member 1