Turnaround time
10 workdays
48.4
40
DNA test for DUMPS / UMPS deficiency in cattle using the UMPS c.1213C>T variant.
Overview
This DNA test examines the UMPS variant c.1213C>T that causes DUMPS. DUMPS stands for Deficiency of Uridine Monophosphate Synthase and is also known as UMPS deficiency or HHD. It is an inherited metabolic disorder in which the UMPS enzyme does not function sufficiently.
The result clarifies whether a bovine is clear, a carrier or has the genetically affected genotype. For breeders, carrier detection is especially important: avoiding carrier pairings helps reduce DUMPS-related embryonic loss while still allowing valuable carrier animals to be used responsibly in a breeding programme.
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 UMPS DUMPS variant were detected. This animal does not create DUMPS risk through this variant in breeding and will not pass this variant on.
Genotype / allele combination: N/DUMPS - carrier
One copy of the tested UMPS DUMPS variant was detected. This animal is a carrier and appears normal, but can pass the variant on; carrier x carrier matings create a risk of embryonic death.
Genotype / allele combination: DUMPS/DUMPS - non-viable genotype
Two copies of the tested UMPS DUMPS variant were detected. This genotype causes complete UMPS deficiency and is embryonic lethal; living homozygous animals are not expected.
Sampling and submission guidelines






References