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Gene information for F7 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID2155
Official gene symbolF7
Full namecoagulation factor VII (serum prothrombin conversion accelerator)
Aliases,-,
Gene summaryThis gene encodes coagulation factor VII which is a vitamin K-dependent factor essential for hemostasis. This factor circulates in the blood in a zymogen form, and is converted to an active form by either factor IXa, factor Xa, factor XIIa, or thrombin by minor proteolysis. Upon activation of the factor VII, a heavy chain containing a catalytic domain and a light chain containing 2 EGF-like domains are generated, and two chains are held together by a disulfide bond. In the presence of factor III and calcium ions, the activated factor then further activates the coagulation cascade by converting factor IX to factor IXa and/or factor X to factor Xa. Alternative splicing of this gene results in 2 transcripts. Defects in this gene can cause coagulopathy. [provided by RefSeq]
LocationChromosome: 13   Locus: 13q34
Gene position113760105 - 113774995  Map Viewer
Gene orientationplus
Gene size14891 bp
Gene sequence