Turnaround time
10 workdays
48.4
40
DNA test for the NDRG1 c.293G>T variant causing Alaskan Malamute polyneuropathy (AMPN).
Overview
This genetic test analyses the NDRG1 c.293G>T variant for polyneuropathy / AMPN in the Alaskan Malamute. NDRG1 is important for normal Schwann-cell and myelin function in peripheral nerves.
AMPN is an inherited polyneuropathy affecting peripheral nerves and myelin. Affected dogs can develop exercise intolerance, abnormal gait, hindlimb weakness, muscle loss, voice change, noisy breathing or laryngeal involvement at a young age. The condition is also described as Alaskan Malamute polyneuropathy, hereditary polyneuropathy and a Charcot-Marie-Tooth-like neuropathy model.
The trait is inherited as an autosomal recessive condition. Clear dogs have two normal copies. Carriers have one copy of the variant and can pass it on. Dogs with two copies have the genotype that causes AMPN.
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 (G/G)
The dog has genotype G/G. The tested NDRG1 c.293G>T variant was not detected and this dog will not pass on this variant.
Genotype / allele combination: Carrier (G/T)
The dog has genotype G/T. This animal is a carrier of the tested NDRG1 c.293G>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 NDRG1-related Alaskan Malamute polyneuropathy.
Sampling and submission guidelines





References