Turnaround time
10 workdays
72.6
60
DNA risk panel for four EAOD-associated markers in USP31, HS3ST2 and RBBP6 in the Border Collie.
Overview
This DNA panel analyses four genetic markers on chromosome 6 used for Adult-onset deafness, also known as Early Adult Onset Deafness, EAOD, early adult hearing loss, progressive early adult deafness or inherited hearing decline in the Border Collie. The markers are located in or near USP31, HS3ST2 and RBBP6.
This is a risk panel rather than a simple affected-or-clear test. The four markers together provide information about inherited susceptibility to EAOD. The overall pattern across all subanalyses is therefore most useful for breeders and owners who want to manage hearing loss risk in Border Collie lines.
EAOD is not congenital deafness. Hearing loss develops gradually in young adult dogs and is often noticed in Border Collies around three to five years of age, when the dog responds less reliably to voice commands, whistles, environmental sounds or sounds at a distance. For working and sporting Border Collies, even moderate hearing loss can have a major practical impact because timing, direction and tone recognition matter in training, herding and daily handling.
Early signs can be subtle: slower response to recall, fewer greetings, stronger startle reactions, changes in barking or uncertainty when sounds are difficult to locate. Many dogs may already have been used for breeding before obvious signs appear, which makes DNA information valuable before selection and mating decisions are made.
Each subanalysis reports whether the dog carries zero, one or two copies of the relevant EAOD risk marker. A dog with one or two copies has a less favourable genetic risk profile for that marker than a dog in which the marker is not detected. The exact risk percentage for each separate marker is not fixed; the result is most useful when the four markers are evaluated together.
The panel helps make accumulation of risk markers visible. This is particularly valuable in breeding plans: dogs with an unfavourable marker pattern can preferably be paired with dogs clear for the relevant markers, helping breeders manage the chance of offspring with an unfavourable EAOD profile.
Included subanalyses
This analysis includes the following subanalyses:
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: No AOD1 risk marker (N/N)
The AOD1 risk marker was not detected. For this specific marker, the dog has the most favourable profile within the EAOD panel.
Genotype / allele combination: One copy of AOD1 risk marker (N/AOD1)
One copy of the AOD1 risk marker was detected. This increases attention to EAOD risk within the panel; combine this information with the other three markers for breeding plans and line management.
Genotype / allele combination: Two copies of AOD1 risk marker (AOD1/AOD1)
Two copies of the AOD1 risk marker were detected. This gives a clearly unfavourable EAOD risk signal for this marker. In breeding plans, pairing with dogs clear for this marker is preferred.
Genotype / allele combination: No AOD2 risk marker (N/N)
The AOD2 risk marker was not detected. For this specific marker, the dog has the most favourable profile within the EAOD panel.
Genotype / allele combination: One copy of AOD2 risk marker (N/AOD2)
One copy of the AOD2 risk marker was detected. This increases attention to EAOD risk within the panel; combine this information with the other three markers for breeding plans and line management.
Genotype / allele combination: Two copies of AOD2 risk marker (AOD2/AOD2)
Two copies of the AOD2 risk marker were detected. This gives a clearly unfavourable EAOD risk signal for this marker. In breeding plans, pairing with dogs clear for this marker is preferred.
Genotype / allele combination: No AOD3 risk marker (N/N)
The AOD3 risk marker was not detected. For this specific marker, the dog has the most favourable profile within the EAOD panel.
Genotype / allele combination: One copy of AOD3 risk marker (N/AOD3)
One copy of the AOD3 risk marker was detected. This increases attention to EAOD risk within the panel; combine this information with the other three markers for breeding plans and line management.
Genotype / allele combination: Two copies of AOD3 risk marker (AOD3/AOD3)
Two copies of the AOD3 risk marker were detected. This gives a clearly unfavourable EAOD risk signal for this marker. In breeding plans, pairing with dogs clear for this marker is preferred.
Genotype / allele combination: No AOD4 risk marker (N/N)
The AOD4 risk marker was not detected. For this specific marker, the dog has the most favourable profile within the EAOD panel.
Genotype / allele combination: One copy of AOD4 risk marker (N/AOD4)
One copy of the AOD4 risk marker was detected. This increases attention to EAOD risk within the panel; combine this information with the other three markers for breeding plans and line management.
Genotype / allele combination: Two copies of AOD4 risk marker (AOD4/AOD4)
Two copies of the AOD4 risk marker were detected. This gives a clearly unfavourable EAOD risk signal for this marker. In breeding plans, pairing with dogs clear for this marker is preferred.
Sampling and submission guidelines






References