Turnaround time
10 workdays
48.4
40
DNA test for the TECPR2 c.4009C>T variant causing juvenile neuroaxonal dystrophy (NAD) in Spanish Water Dogs.
Overview
This genetic test analyses the TECPR2 c.4009C>T variant for neuroaxonal dystrophy, also known as NAD / TECPR2-related juvenile NAD, in Spanish Water Dogs.
Neuroaxonal dystrophy is an inherited neurological disorder in which nerve pathways in the brain, spinal cord or peripheral nervous system become damaged. As a result, communication between nerve cells and muscles becomes progressively disrupted.
In Spanish Water Dogs, this juvenile NAD form is characterised by neurological deficits, gait abnormalities, behavioural changes and progressive cognitive and motor decline. Signs usually begin at around 6 to 18 months.
Typical signs can include loss of coordination, ataxia, tremor, weakness, abnormal posture, toe dragging, behavioural changes, vision problems or a rapidly progressive neurological presentation. Some NAD forms start in very young puppies; other variants become visible later in life.
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 NAD.
For this breed, the test helps manage carriers before the variant spreads unnoticed through breeding lines.
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 (C/C)
The dog has genotype C/C. The tested TECPR2 c.4009C>T variant was not detected and this dog will not pass on this variant.
Genotype / allele combination: Carrier (C/T)
The dog has genotype C/T. This animal is a carrier of the tested TECPR2 c.4009C>T variant and can pass it to offspring. One copy does not cause this autosomal recessive disorder.
Genotype / allele combination: Affected genetic result (T/T)
The dog has genotype T/T. This genotype causes the tested autosomal recessive form of TECPR2-related juvenile neuroaxonal dystrophy.
Sampling and submission guidelines





References