Turnaround time
10 workdays
48.4
40
DNA test for Hereditary nasal parakeratosis / HNPK in the Greyhound, analyzing the SUV39H2 variant c.996+3_996+6delAAGT.
Overview
This genetic test analyzes the SUV39H2 variant c.996+3_996+6delAAGT for Hereditary nasal parakeratosis / HNPK in the Greyhound. The condition is also described as hereditary nasal parakeratosis, HNPK, nasal parakeratosis, dry nose, crusty nose and SUV39H2-related keratinization disorder.
HNPK is an inherited skin disorder in which keratinization of the nasal planum is abnormal. Affected Greyhounds can develop hard, scaly crusts, dry thickening, painful fissures and chronic irritation on the nose. The SUV39H2 gene is involved in regulating keratinocyte differentiation; disruption of this process explains why the nose is mainly affected.
The trait is inherited as an autosomal recessive condition. Dogs with two copies of the tested variant are expected to be affected. Carriers have one copy, often look healthy and can still pass the variant on.
Testing is useful for Greyhounds selected for breeding, dogs from lines with nasal problems and when a dry, crusted nose needs a genetic explanation. Because carriers usually have no visible skin signs, DNA testing helps identify hidden variants in a line in time.
The test makes hidden carrier status visible and helps breeders, veterinarians and owners make decisions based on concrete genetic information.
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 (N/N)
The tested variant was not detected. This dog will not develop this condition because of this variant and will not pass this variant to offspring.
Genotype / allele combination: Carrier (N/delAAGT)
This dog carries one copy of the tested variant. A carrier will not develop this autosomal recessive condition from one copy, but can pass the variant on; mating two carriers can produce affected puppies.
Genotype / allele combination: Affected (delAAGT/delAAGT)
This genotype causes HNPK for the tested Greyhound variant. The dog has two copies of the SUV39H2 deletion and can develop dry, crusted nasal changes, fissures and chronic irritation; the variant will be passed to all offspring.
Sampling and submission guidelines





References