Turnaround time
10 workdays
48.4
40
Genetic test for the NDRG1 c.1080_1089del10 variant for Early Onset Progressive Polyneuropathy (EOPP/GHPN) in Greyhounds.
Overview
This genetic test analyses the NDRG1 variant c.1080_1089del10 for Early Onset Progressive Polyneuropathy in the Greyhound. The condition is also known as EOPP, Greyhound Polyneuropathy, GHPN and juvenile Greyhound polyneuropathy. The test determines whether the dog is clear, a carrier or genetically affected for this autosomal recessive variant.
EOPP is an inherited neurological disorder in which the peripheral nerves do not function properly. In affected young Greyhounds, first signs may appear from about three to nine months of age. Typical signs include exercise intolerance, abnormal gait, high-stepping movement, trembling or collapse after activity, progressive muscle weakness, ataxia, voice changes and, in severe cases, breathing difficulties.
The condition is inherited as autosomal recessive. A dog with N/N does not carry the variant. A dog with N/del is a carrier and can pass the variant to offspring. A dog with del/del has two copies and develops the tested inherited form of Greyhound polyneuropathy.
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: N/N - clear
This Greyhound does not carry the tested NDRG1 deletion. The dog will not develop EOPP/GHPN due to this variant and will not pass this variant on.
Genotype / allele combination: N/del - carrier
This Greyhound carries one copy of the NDRG1 deletion. The dog is a carrier, will not develop EOPP/GHPN due to this recessive variant, but can pass the variant on.
Genotype / allele combination: del/del - affected
This Greyhound has two copies of the NDRG1 deletion. This genotype causes the tested inherited form of EOPP/GHPN.
Sampling and submission guidelines





References