Genetic Test
The F7 (Coagulation Factor VII) gene encodes coagulation factor VII, a vitamin K-dependent protein essential for blood clotting.
This protein circulates in the bloodstream and plays a critical role in activating the coagulation cascade to stop bleeding.
Mutations in the F7 gene can lead to factor VII deficiency, a bleeding disorder characterized by impaired blood clotting.
This genetic test targets a specific mutation associated with factor VII deficiency.
Disease Description
Factor VII deficiency is a hereditary bleeding disorder caused by impaired blood clotting activity due to a deficiency of coagulation factor VII.
This condition is sometimes referred to as hemophilia.
Affected animals may suffer from prolonged bleeding at sites of trauma, the umbilical cord after birth, as well as spontaneous bleeding from the nose, mouth, eyes, and other areas.
