| Health / Medical Topics |
F2 wt Allele
Human F2 wild-type allele is located in the vicinity of 11p11 and is approximately 20 kb in length. This allele, which encodes prothrombin protein, is involved in the regulation of coagulation. Mutation of the gene is associated with dysprothrombinemia and genetic variation may affect susceptibility to ischemic stroke. (NCI Thesaurus)
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The determination of the amount of F2 isoprostane present in a urine sample.
A protein encoded by the F2 gene.
This gene plays a role in the coagulation cascade.
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Human F12 wild-type allele is located within 5q33-qter and is approximately 8 kb in length. This allele, which encodes coagulation factor XII…
This gene is involved in blood coagulation and fibrinolysis.
