DNA & genetic tests
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48.4

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40

Progressive retinal atrophy / rcd1a-PRA (PDE6B-related) - Sloughi

Genetic test for the PDE6B c.2448_2449insTGAAGTCC variant that causes rcd1a-PRA in the Sloughi.

Turnaround time
10 workdays
test Methods
Sequencing
Test code
PVT-37AB575443EB
Species
Dog
Breeds
Sloughi
Matrices
Blood, Blood (EDTA), Blood (Heparin), Swab, Tissue

Overview

What does this test examine?

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.

What does this condition mean?

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.

Inheritance and result

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.

  • N/N - no copy of the tested variant detected.
  • N/insTGAAGTCC - carrier: one copy of the tested variant detected.
  • insTGAAGTCC/insTGAAGTCC - affected genotype: two copies of the tested variant detected.

Practical value of 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:

  • Progressive retinal atrophy / rcd1a-PRA (PDE6B-related) - Sloughi

Allele combinations & result interpretations

Sampling and submission guidelines

References