LABOKLIN (UK)| Genetic Diseases | Dogs| Progressive Retinal Atrophy (CNGA1 PRA)
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Progressive Retinal Atrophy (CNGA1 PRA)

Test number: 8375
Gene: CNGA1
Price: £ 48.00 (including VAT)
Laboklin response to the statement issued by the Norwegian Shetland Sheepdog Club
Breed
Shetland Sheepdog (Sheltie) .
Kennel Club
This test is part of the Official UK Kennel Club DNA Testing Scheme in Shetland Sheepdog (Sheltie).

for UK registered dogs, Laboklin can send results of the tests which are part of the Official UK Kennel Club DNA testing scheme to the Kennel Club (KC) to be recorded and published as part of the Kennel Club scheme. Results will only be recorded and published by the KC if the result report includes the dog’s microchip or tattoo number along with either the dog’s registered name or registered number. Any test results that do not carry these identifying features will not be recorded by the Kennel Club.

In order to ensure that test results are sent to the Kennel Club, customers must also sign the declaration section on the order form to give Laboklin permission to do so.

important: When you sign the declaration, Laboklin will send the results to the KC on your behalf, and you do not need to send them to the KC yourself again to avoid unnecessary duplications.

The Disease
Progressive retinal atrophy (PRA) refers to a group of genetic disease that occur in a number of dog breeds. The disease is characterised by vision impairment caused by degeneration of the retina in both eyes leading to blindness. The mutation responsible for this disease has already been identified in a number of breeds and DNA tests have been developed to enable breeders to avoid breeding affected dogs. PRA in shelties is clinically similar to PRA in other breeds but the mutation leading to the disease in shelties was not identified. In a recent study scientists found that in shelties there is more than one PRA variant.Scientists have been able to identify one of the mutations that causes PRA in this breed and a DNA test is now available from Laboklin.

In Shelties, the disease shows a varying age on onset. In a study on affected shelties, PRA was diagnosed between the age of 2 and 11.

PRA in shelties is recessive which means that a dog will only develop the disease when it inherits two copies of the mutation, one from each parent. If a dog inherits one copy of the mutant gene from one parent and one copy of the healthy gene from the other parent, it will not develop the disease associated with this mutation but it can pass the mutation to its offspring.

A dog that carries one copy of the mutation (carrier) will not be affected by this mutation but it should only be bred to a clear dog.

The DNA test enable breeders to identify if the dog is clear, carrier or affected and plan their breeding program to avoid having affected puppies.

It is important to point out that this test detects the mutation that causes one variant of PRA. There is at least one more, yet unidentified, mutation responsible for other PRA variant(s) in shelties, which is not detected by this test. The breed also suffers from an additional form of retinal degeneration called Slow Progressing Retinopathy ( SPR ) that progresses more slowly and does not cause such obvious visual impairment as does PRA (Karlstam et al. 2011). This test does not detect SPR. The test is useful to eliminate one form of PRA.

Trait of Inheritance
.

Inheritance : AUTOSOMAL RECESSIVE trait


 

Sire

 

Dam

 

Offspring

         
clear
clear
100% clear
         
clear
carrier
50%  clear + 50% carriers
         
clear
affected
100% carriers
         
carrier
clear
50%  clear + 50% carriers
         
carrier
carrier
25% clear + 25% affected + 50% carriers
         
carrier
affected
50% carriers + 50% affected
         
affected
clear
100%  carriers
         
affected
carrier
50% carriers + 50% affected
         
affected
affected
100% affected

 


Clear

Genotype: N / N [ Homozygous normal ]

The dog is noncarrier of the mutant gene.

It is very unlikely that the dog will develop Progressive Retinal Atrophy (CNGA1 PRA). The dog will never pass the mutation to its offspring, and therefore it can be bred to any other dog.

 

Carrier

Genotype: N / CNGA1 [ Heterozygous ]

The dog carries one copy of the mutant gene and one copy of the normal gene.

It is very unlikely that the dog will develop Progressive Retinal Atrophy (CNGA1 PRA) but since it carries the mutant gene, it can pass it on to its offspring with the probability of 50%.

Carriers should only be bred to clear dogs.

Avoid breeding carrier to carrier because 25% of their offspring is expected to be affected (see table above)

 

Affected

Genotype: CNGA1 / CNGA1 [ Homozygous mutant ]

 

The dog carries two copies of the mutant gene and therefore it will pass the mutant gene to its entire offspring.

The dog is likely to develop Progressive Retinal Atrophy (CNGA1 PRA) and will pass the mutant gene to its entire offspring
Sample Requirements
Whole blood in EDTA tube (0.5 - 1 ml) or Buccal Swabs.
Turnaround
1-3 weeks
Price
£ 48.00 (including VAT)

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