Turnaround time
10 workdays
48.4
40
DNA test for Hypotrichosis / HY in Hereford cattle using the KRT71 c.281_288del variant.

Overview
This DNA test examines the KRT71 variant c.281_288del that causes congenital hypotrichosis, also known as HY, in Hereford cattle. Hypotrichosis means clearly reduced hair growth. Affected calves may be born hairless or nearly hairless and usually develop a very short, fine, woolly, rough or curly coat.
The result helps breeders distinguish clear animals, carriers and genetically affected animals. This supports avoidance of carrier pairings, management of the variant in the breeding population and confirmation of the hereditary cause of abnormal hair growth in Hereford cattle.
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: N/N - clear
No copies of the tested KRT71 HY variant were detected. This animal will not develop KRT71-related HY due to this variant and will not pass this variant to offspring.
Genotype / allele combination: N/HY - carrier
One copy of the tested KRT71 HY variant was detected. This animal is a carrier and is normally not affected, but can pass the variant to about half of its offspring.
Genotype / allele combination: HY/HY - genetically affected
Two copies of the tested KRT71 HY variant were detected. This genotype causes congenital hypotrichosis with clearly reduced or abnormal hair growth in Hereford cattle.
Sampling and submission guidelines






References