abnormality of prothrombin Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of clotting factor II, which is known as prothrombin, a vitamin K-dependent proenzyme that functions in the blood coagulation cascade. (Human Phenotype Ontology, HP_0012200)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012200
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7 genes associated with the abnormality of prothrombin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
F10 coagulation factor X
F2 coagulation factor II (thrombin)
GFI1B growth factor independent 1B transcription repressor
GGCX gamma-glutamyl carboxylase
PMM2 phosphomannomutase 2
PRF1 perforin 1 (pore forming protein)
VKORC1 vitamin K epoxide reductase complex, subunit 1