Turnaround time
10 workdays
48.4
40
DNA test for bovine leukocyte adhesion deficiency, BLAD or HHB in cattle using the ITGB2 c.383A>G variant.

Overview
This DNA test examines the ITGB2 variant c.383A>G that causes bovine leukocyte adhesion deficiency. The condition is also known as BLAD, leukocyte adhesion deficiency type I or Haplotype HHB. ITGB2 encodes CD18, a component of beta-2 integrins on white blood cells.
The result helps breeders distinguish clear animals, carriers and genetically affected animals. For Holstein-Friesian and other at-risk breeds, carrier detection is valuable for removing BLAD from breeding lines while retaining valuable animals responsibly.
BLAD is inherited as an autosomal recessive disorder.
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 ITGB2 BLAD variant were detected. This animal will not develop BLAD due to this variant and will not pass this variant on.
Genotype / allele combination: N/BLAD - carrier
One copy of the tested ITGB2 BLAD variant was detected. This animal is a carrier and is generally healthy itself, but can pass the variant on; carrier x carrier matings create a risk of calves with BLAD.
Genotype / allele combination: BLAD/BLAD - genetically affected
Two copies of the tested ITGB2 BLAD variant were detected. This genotype causes BLAD: white blood cells do not function properly, making calves highly susceptible to severe infections.
Sampling and submission guidelines






References