Turnaround time
10 workdays
48.4
40
DNA test for cholesterol deficiency, HCD or CDH in cattle using the APOB 1.3 kb ERV2-1 insertion.
Overview
This DNA test examines the APOB1.3 kb ERV2-1 insertion that causes cholesterol deficiency. The disorder is also known as HCD, CDH, Holstein cholesterol deficiency or cholesterol deficiency haplotype. APOB is essential for transport of fats and cholesterol in the body.
The result helps distinguish clear animals, carriers and genetically affected animals. In Holstein-related breeding lines, carrier detection is important to prevent losses from affected calves and plan matings more precisely.
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 APOB HCD variant were detected. This animal will not develop cholesterol deficiency due to this variant and will not pass this variant on.
Genotype / allele combination: N/HCD - carrier
One copy of the tested APOB HCD variant was detected. This animal is a carrier and can pass the variant on; carrier x carrier matings create a risk of calves with severe cholesterol deficiency.
Genotype / allele combination: HCD/HCD - genetically affected
Two copies of the tested APOB HCD variant were detected. This genotype causes severe cholesterol deficiency with impaired fat transport, chronic diarrhoea, reduced growth and a high chance of death at young age.
Sampling and submission guidelines






References