Turnaround time
10 workdays
48.4
40
DNA test for Leukoencephalomyelopathy / LEMP, analysing NAPEPLD c.538G>C.
Overview
This genetic test analyses the NAPEPLD c.538G>C variant in the Leonberger. The condition is described as leukoencephalomyelopathy, LEMP and NAPEPLD-related white matter disease.
LEMP is a severe disorder of the white matter in the central nervous system. Dogs can develop progressive gait abnormalities, knuckling, paw dragging, hypermetria, ataxia and increasing mobility restriction.
The trait is inherited in an autosomal recessive manner. One copy means carrier status. Two copies mean the genotype interpreted as affected or high risk for this disorder in the known breed context.
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 NAPEPLD c.538G>C (G/G)
The dog does not carry the tested NAPEPLD variant. It will not develop LEMP in the Leonberger due to this variant and will not pass this specific variant on.
Genotype / allele combination: Carrier of NAPEPLD c.538G>C (G/C)
The dog carries one copy of the tested NAPEPLD variant. This is a carrier result: the dog is generally not affected, but can pass the variant to offspring.
Genotype / allele combination: Two copies of NAPEPLD c.538G>C (C/C)
The dog has two copies of the tested NAPEPLD variant. This genotype causes LEMP in the Leonberger in the known breed context and is important for breeding selection.
Sampling and submission guidelines





References