Turnaround time
10 workdays
48.4
40
Genetic test for the PRKDC c.10879G>T variant that causes severe combined immunodeficiency / SCID in the Jack Russell Terrier.
Overview
This genetic test analyses the PRKDC c.10879G>T variant in the Jack Russell Terrier. The condition is known as severe combined immunodeficiency, SCID and PRKDC-related SCID. The result shows whether the dog carries zero, one or two copies of the tested variant.
PRKDC is required for normal development of the adaptive immune system. When both gene copies carry the tested variant, puppies cannot build an effective immune response and become highly vulnerable to infection.
SCID is a severe inherited immune disorder. Affected puppies can fail to thrive, lose weight, become lethargic, develop chronic or recurrent diarrhoea and be highly susceptible to bacterial, viral and fungal infections. In this condition, infections can quickly become severe or life-threatening.
Because SCID can appear early in life and carriers can look healthy, DNA testing is especially valuable before breeding decisions. The result identifies carrier animals and helps prevent at-risk matings.
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 genotype that causes this form of SCID.
This test is important because carriers cannot be recognised by appearance. Breeders can use the result to select safe matings and prevent puppies with two copies of the variant.
For breed clubs and breeding programmes, the test helps actively reduce a severe, often life-limiting immune disorder while managing healthy carriers responsibly.
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 (GG)
No copy of the tested PRKDC variant was detected. This dog will not develop this disorder from the tested variant and will not pass it to offspring.
Genotype / allele combination: Carrier (GT)
This dog carries one copy of the tested PRKDC variant and can pass it on. The dog is expected to be unaffected, but mating with another carrier can produce affected puppies.
Genotype / allele combination: Affected genotype (TT)
This dog has two copies of the tested PRKDC variant. This genotype causes the disorder in the breed or test context for which this analysis is intended. The dog will pass the variant to all offspring.
Sampling and submission guidelines





References