Turnaround time
10 workdays
48.4
40
Genetic test for the HCRTR2 variant c.1105+5G>A that causes narcolepsy with cataplexy in the Labrador Retriever.
Overview
This genetic test analyses the HCRTR2 variant c.1105+5G>A in the Labrador Retriever. The condition is known as narcolepsy, familial narcolepsy, narcolepsy with cataplexy or a sleep-wake disorder.
Affected dogs can suddenly lose muscle control, collapse or show brief sleep episodes. Attacks are often triggered by food, play or excitement. For breeders this matters because carriers can look healthy while still passing the variant to offspring.
The trait is autosomal recessive. A dog without the variant is clear, a dog with one copy is a carrier and a dog with two copies is genetically affected for this HCRTR2-related form of narcolepsy.
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)
This dog does not carry the tested HCRTR2 variant and will not pass this variant to offspring.
Genotype / allele combination: Carrier (G/A)
This dog carries one copy of the tested HCRTR2 variant. It is a carrier and can pass the variant on; mating with another carrier can produce genetically affected puppies.
Genotype / allele combination: Genetically affected (A/A)
This dog carries two copies of the tested HCRTR2 variant. This genotype causes the tested autosomal recessive form of narcolepsy with cataplexy.
Sampling and submission guidelines





References