antithrombin iii deficiency Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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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23 genes co-occuring with the disease antithrombin iii deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
SERPINC1 serpin peptidase inhibitor, clade C (antithrombin), member 1 2.55559
F5 coagulation factor V (proaccelerin, labile factor) 1.9741
PROS1 protein S (alpha) 1.95488
F2 coagulation factor II (thrombin) 1.47857
MTHFR methylenetetrahydrofolate reductase (NAD(P)H) 1.23343
SERPIND1 serpin peptidase inhibitor, clade D (heparin cofactor), member 1 1.23212
PLG plasminogen 1.04504
PROC protein C (inactivator of coagulation factors Va and VIIIa) 0.774523
COX5A cytochrome c oxidase subunit Va 0.670333
ASRGL1 asparaginase like 1 0.658818
SERPINF2 serpin peptidase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 2 0.595623
F3 coagulation factor III (thromboplastin, tissue factor) 0.578883
F8 coagulation factor VIII, procoagulant component 0.471468
FAM155B family with sequence similarity 155, member B 0.454847
F9 coagulation factor IX 0.404557
F7 coagulation factor VII (serum prothrombin conversion accelerator) 0.336876
PMM2 phosphomannomutase 2 0.332121
F12 coagulation factor XII (Hageman factor) 0.328469
PROCR protein C receptor, endothelial 0.296571
PLAT plasminogen activator, tissue 0.281868
SERPINB1 serpin peptidase inhibitor, clade B (ovalbumin), member 1 0.266558
TPT1 tumor protein, translationally-controlled 1 0.220081
PPBP pro-platelet basic protein (chemokine (C-X-C motif) ligand 7) 0.211261