F9 wt Allele
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F9 wt Allele Definition
Human F9 wild-type allele is located within Xq27.1-q27.2 and is approximately 33 kb in length. This allele, which encodes coagulation factor IX protein, plays a role in the intrinsic blood coagulation cascade. Alterations of this gene, including point mutations, insertions and deletions, cause factor IX deficiency. This is a recessive X-linked disorder, also called hemophilia B or Christmas disease.
F9 wt Allele Synonyms
F9 wt Allele, Coagulation Factor IX (Plasma Thromboplastic Component, Christmas Disease, Hemophilia B) wt Allele, FIX, HEMB, PTC
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