Turnaround time
10 workdays
48.4
40
DNA test for KCNJ10 c.627C>G, the recessive variant causing SCA, SDCA1 and ataxia with myokymia or seizures in terrier-type dogs and Dachshunds.
Overview
This genetic test analyses the KCNJ10 variant c.627C>G in the terrier-type dogs and Dachshunds. The condition is known as spinocerebellar ataxia, SDCA1 or SAMS, SCA and hereditary cerebellar ataxia.
Affected dogs usually develop coordination loss, unsteady gait, balance problems and neurological signs at a young age. This KCNJ10 form can also include myokymia, neuromyotonia or seizure-like episodes, making the result important for both breeding plans and interpretation of early neurological signs.
The trait is autosomal recessive. Clear dogs do not carry the tested variant, carriers have one copy and affected dogs have two copies. Carriers are usually clinically normal 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 for the tested KCNJ10 variant (CC)
The dog does not carry the tested variant and will not pass this variant to offspring.
Genotype / allele combination: Carrier of the tested KCNJ10 variant (CG)
The dog carries one copy of the variant. It is usually not affected, but can pass the variant on; mating with another carrier can produce puppies with SCA / SDCA1.
Genotype / allele combination: Affected genotype for SCA / SDCA1 (GG)
The dog has two copies of the variant. This genotype causes SCA / SDCA1 with severe coordination and movement problems.
Sampling and submission guidelines





References