Turnaround time
10 workdays
48.4
40
DNA test for the complete CNGB3 deletion that can cause achromatopsia 3, cone degeneration and day blindness in dogs.
Overview
This genetic test examines a complete deletion of the CNGB3 gene. This variant is known in achromatopsia 3, also called cone degeneration, hemeralopia or day blindness.
CNGB3 is important for cone function in the retina. Affected dogs can have clear problems in bright light: day blindness, light sensitivity, reduced colour vision and reduced visual acuity. Vision in dim light is often much better preserved because the cone system is mainly affected.
The condition is inherited as an autosomal recessive trait. A dog with two copies of the deletion develops the disorder; a carrier usually has normal vision but can pass the variant to offspring.
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: Clear / normal genotype
The dog does not carry the tested variant for achromatopsia 3 / day blindness. This animal will not pass this specific variant to offspring.
Genotype / allele combination: Carrier
The dog carries one copy of the tested variant for achromatopsia 3 / day blindness. Carriers are generally not clinically affected, but can pass the variant on; pairing two carriers can produce affected puppies.
Genotype / allele combination: Affected / genetically positive
The dog has two copies of the tested CNGB3 deletion. This genotype causes achromatopsia 3 with day blindness and light sensitivity; the animal will pass the deletion to all offspring.
Sampling and submission guidelines





References