Turnaround time
10 workdays
48.4
40
DNA test for the SERPINB11 c.504_505insC variant that causes autosomal recessive hoof wall separation disease / HWSD in horses.
Overview
This genetic test analyses the SERPINB11 c.504_505insC variant in horses. The condition is also known as Hoof Wall Separation Disease, HWSD, hoof wall separation syndrome and an inherited disorder of hoof horn integrity.
HWSD affects the quality and attachment of the hoof wall. In affected horses, the weight-bearing hoof wall can separate, crumble or lack strength. This can cause pain, lameness, difficulty bearing weight and intensive hoof care needs. The condition is best known in Connemara ponies, but related or historically connected lines can also be relevant.
The test clarifies whether a horse is clear, carrier or has two copies of the HWSD variant. Carriers are usually healthy themselves but can pass the variant on. Identifying carriers helps breeders plan healthy matings without automatically excluding valuable bloodlines.
HWSD is inherited as autosomal recessive. A horse with one copy is a carrier and passes the variant to about half of its offspring. Two copies cause HWSD and can lead to severe hoof wall abnormalities.
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 / N/N
No copy of the tested SERPINB11 variant was detected. This horse will not develop HWSD due to this variant and does not pass it on.
Genotype / allele combination: Carrier / N/HWSD
This horse carries one copy of the HWSD variant. A carrier normally does not develop HWSD from this recessive variant, but can pass it to offspring.
Genotype / allele combination: Affected / HWSD/HWSD
This genotype causes HWSD. Horses with two copies can develop severe hoof wall separation with pain, lameness and intensive hoof care needs.
Sampling and submission guidelines







References