Turnaround time
10 workdays
48.4
40
Genetic test for the PDE6B c.2448_2449insTGAAGTCC variant that causes rcd1a-PRA in the Sloughi.
Overview
This genetic test analyses the PDE6B c.2448_2449insTGAAGTCC variant in the Sloughi. The condition is known as progressive retinal atrophy / rcd1a-PRA and is also referred to as PRA, rcd1a, rcd1a-PRA and rod-cone dysplasia 1a. The result shows whether the dog carries zero, one or two copies of the tested variant.
PDE6B is important for normal photoreceptor function in the retina. When both gene copies carry the tested variant, this causes an inherited form of retinal degeneration with progressive loss of vision.
rcd1a-PRA is characterised by reduced dark vision and visual-field defects that can progress to blindness. The test is specifically relevant for Sloughi lines in which this PDE6B insertion occurs.
In progressive retinal atrophy, the light-sensitive retinal cells lose function. Dogs may first show reduced vision in dim light or bright light, become less confident in unfamiliar surroundings, bump into objects and eventually become severely visually impaired or blind.
The trait is inherited in an autosomal recessive way. A clear dog does not carry the variant. A carrier has one copy and is usually not affected, but can pass the variant to offspring. A dog with two copies has the affected genotype for this test.
This DNA test is useful because carriers can look completely normal. Breeders can use the result to plan matings more precisely, manage carriers responsibly and strongly reduce the risk of puppies affected by inherited retinal degeneration.
The result also makes eye health easier to manage within a breeding programme: it can support puppy selection, breeding-animal evaluation, comparison of possible mates and long-term planning across generations. In a less common breed such as the Sloughi, clear carrier status helps combine genetic diversity with health-focused selection.
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 (N/N)
No copy of the tested PDE6B variant was detected. This dog will not develop this form of progressive retinal atrophy / rcd1a-PRA from the tested variant and will not pass it to offspring.
Genotype / allele combination: Carrier (N/insTGAAGTCC)
This dog carries one copy of the tested PDE6B variant and can pass it on. The dog is expected to be unaffected, but mating with another carrier can produce puppies with two copies.
Genotype / allele combination: Affected genotype (insTGAAGTCC/insTGAAGTCC)
This dog has two copies of the tested PDE6B variant. This genotype causes progressive retinal atrophy / rcd1a-PRA in the breed context for which this test is intended; the dog will pass the variant to all offspring.
Sampling and submission guidelines





References