Turnaround time
10 workdays
48.4
40
Genetic test for F9 c.383G>A, an X-linked recessive variant that causes haemophilia B or factor IX deficiency in cats.
Overview
This genetic test examines the F9 variant c.383G>A. Haemophilia B is also known as factor IX deficiency or Christmas disease. The F9 gene encodes clotting factor IX, a protein needed for blood to clot efficiently.
Cats with an affected genotype can produce too little functional factor IX. As a result, blood may clot poorly and bleeding can continue for longer after injury, surgery, dental procedures or birth. Bruising, delayed bleeding and internal bleeding may also be part of the condition.
The F9 gene is located on the X chromosome. Male cats have one X chromosome and become affected when that X chromosome carries the variant. Female cats with one variant copy are carriers and can pass the variant on; female cats with two variant copies can also be affected.
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
The tested F9 variant was not detected. This result gives no genetic indication of haemophilia B caused by this variant.
Genotype / allele combination: Carrier
One copy of the tested F9 variant was detected. In a female cat this means carrier status and she can pass the variant on; in a male cat, presence of an X-linked variant should be handled as an affected result according to genotype entry.
Genotype / allele combination: Affected
The tested F9 variant is present in an affected genotype. This causes factor IX deficiency or haemophilia B and increases the risk of prolonged or severe bleeding.
Sampling and submission guidelines





References