Turnaround time
10 workdays
48.4
40
DNA test for the F11 76-bp insertion that causes Factor XI deficiency (FXID) in cattle.

Overview
Factor XI deficiency, also known as FXID, F11 deficiency, plasma thromboplastin antecedent deficiency or Hemophilia C, is an inherited coagulation disorder in cattle. This analysis detects the 76-bp insertion in exon 12 of the F11 gene, described as c.1406ins76.
Factor XI contributes to stable blood clotting. Animals with two copies of the variant can show excessive or prolonged bleeding, for example after dehorning, castration, trauma or from the umbilical cord in calves. Bloody milk, poorer reproductive performance and increased vulnerability in the herd have also been described with FXID.
The result helps distinguish clear animals, carriers and affected animals. This is especially useful in Holstein Friesian and Sahiwal cattle, where this variant is described.
For breeders, this supports planned matings and controlled use of carrier animals without losing valuable genetics unnecessarily.
Included subanalyses
This analysis includes the following subanalysis:
Allele combinations & result interpretations
Below, for each tested locus, you will find the possible allele combinations that may be reported within this analysis, together with a brief explanation of their genetic meaning. The interpretation of possible interactions between different loci is included in the report, but is not shown here in full because that would lead to too many combinations on this page. The final expression may also depend on other genes and their interaction.
Genotype / allele combination: Clear
This animal has no copy of the tested F11 insertion. It will not develop Factor XI deficiency due to this variant and will not pass on this FXID variant.
Genotype / allele combination: Carrier
This animal carries one copy of the tested F11 insertion. It can pass on the FXID variant; mating with another carrier can produce calves with Factor XI deficiency.
Genotype / allele combination: Affected
This animal has two copies of the tested F11 insertion. This genotype causes Factor XI deficiency and increases the risk of prolonged or excessive bleeding.
Sampling and submission guidelines






References