Turnaround time
10 workdays
48.4
40
DNA test for the CLN8 c.349dupT insertion causing neuronal ceroid lipofuscinosis 8 (NCL8) in Salukis.
Overview
This genetic test analyses the CLN8 c.349dupT variant for neuronal ceroid lipofuscinosis 8, also known as NCL8, neuronal ceroid lipofuscinosis type 8 and Batten disease, in Salukis.
NCL8 belongs to the neuronal ceroid lipofuscinoses: inherited lysosomal storage diseases in which waste products such as ceroid and lipofuscin accumulate in nerve cells and often in the retina. This leads to progressive neurological signs, loss of vision and declining mobility.
In Salukis, affected dogs often start showing behavioural changes within the first year of life, such as anxiety or restlessness. Reduced vision, hearing problems, tremor, epileptic seizures, walking difficulty and loss of house training can follow.
Common signs include behavioural change, anxiety or restlessness, reduced response to commands, compulsive circling, ataxia, tremor, epileptic seizures, declining vision or hearing and loss of house training. The course is progressive and can already have a major impact on welfare and quality of life at a young age.
The trait is inherited as an autosomal recessive condition. Clear dogs have two normal copies. Carriers have one copy of the tested variant and can pass it on. Dogs with two copies have the genotype that causes this form of NCL8.
For Saluki breeders, this test is especially useful because carriers can look healthy while two carriers together can produce affected puppies.
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 (N/N)
The dog has genotype N/N. The tested CLN8 c.349dupT variant was not detected and this dog will not pass on this variant.
Genotype / allele combination: Carrier (N/dupT)
The dog has genotype N/dupT. This animal is a carrier of the tested CLN8 c.349dupT variant and can pass it to offspring. One copy does not cause this autosomal recessive NCL8 form.
Genotype / allele combination: Affected genetic result (dupT/dupT)
The dog has genotype dupT/dupT. This genotype causes the tested autosomal recessive form of NCL8 in Salukis.
Sampling and submission guidelines





References