Plott
The tested variant with the highest allele frequency is Hypocatalasia, at 8% among the 25 Plotts tested (Donner 2023; gene copies, not dogs), then Progressive Rod-Cone Degeneration (4%) and Factor VII Deficiency (2%).
Which disease variants turn up in Plotts?
From a panel of 250 Mendelian-disease variants screened in 1,054,293 dogs (Donner et al. 2023), 4 turn up in Plotts at observable frequency. The figure beside each is its allele frequency. Of the gene copies tested in this breed, the share that carry the variant. Every dog carries two copies, so this is not the share of dogs. It is not clinical risk. Most recessive variants require two copies for disease expression; many dominant variants show incomplete penetrance. Read this as a population fingerprint of what's in the gene pool, not a per-dog prediction.
CATwhat this gene does
CAT is a gene that helps produce an enzyme called catalase, which breaks down hydrogen peroxide in the body to prevent cell damage.
For your dog: If your dog is from a breed that can carry this gene, it’s worth asking your vet about testing. Being a carrier doesn’t mean your dog is affected, but it can inform health decisions.
PDK4what this gene does
PDK4 helps regulate how cells use energy, especially in the heart muscle.
For your dog: If your dog is one of the breeds known to carry this gene, it’s worth discussing heart health with your vet, but being a carrier doesn’t mean your dog will develop disease.
PRCDwhat this gene does
PRCD is a gene involved in the health of a dog's retina, the part of the eye that detects light and helps with vision.
For your dog: If your dog belongs to a breed known to carry PRCD changes, it's worth discussing eye health and potential genetic testing with your vet.
F7what this gene does
The F7 gene helps produce a protein important for blood clotting, which stops bleeding when dogs get injured.
For your dog: If your dog is from a breed known to carry F7 variants, it's worth mentioning to your vet before any surgery or if you notice unusual bleeding.
What these results mean for a Plott
4.0% of Plotts in the Donner 2023 cohort carried it (n=25).
- This is a marker, not an established cause. The curated record says a test based on it is not a good indicator of heart disease risk even in Dobermans, the breed it was found in.
OMIA 000162-9615
“it is evident that any DNA test based on this marker will not be a good indicator of liability to this disorder in Dobermans” OMIA 000162-9615
What to do
A carrier result for this marker is not, on its own, a reason for heart screening. Heart screening is a conversation with your veterinarian about the breed and the dog.
No test, or a mix
What this marker means in breeds other than the Doberman is not established in the sources this page draws on.
For researchers Population genetics, disease models and every recorded condition Open the research detail for the Plott
Where every number on this page came from.
This page draws on one primary data source. Allele frequencies and sample sizes come from Donner et al. 2023 (CC-BY-4.0), a direct-to-consumer screening cohort, graded Limited as a study design because the dogs were tested at their owners' choice. No genotyped research dogs of this breed are in the three open releases the atlas reads, so the population-genetic sections other breed pages carry are absent here for that reason, not hidden. Conditions recorded for the breed come from OMIA.
What this page does not yet have. Inheritance modes and per-disease penetrance evidence from Donner 2023 are in the structured data for every variant the panel covers. Mondo, OMIM, Ensembl, and HGNC cross-references live on the gene and disease pages this page links to, rather than being repeated here. What is still absent from this breed page is anything not in the cited panel, and each such gap carries its cause where it appears.
How to cite this page. Cite Donner et al. 2023 (doi:10.1371/journal.pgen.1010651) for every frequency on this page, and OMIA for each condition, with the sample size shown beside the figure.
Some things about living with a plott never make it into a database. Add what you know as a Keeper, in your words →
Lived experience, kept beside the science.No plotts are in the atlas yet. Yours would be the first star for the breed.
Every plott added sharpens the breed's genetic neighborhood. Enrollment is free. The data stays open. The star is permanent.
- Donner J, Freyer J, Davison S, Anderson H, Blades M, Honkanen L, et al. (2023). Genetic prevalence and clinical relevance of canine Mendelian disease variants in over one million dogs. PLOS Genetics 19(2):e1010651. doi:10.1371/journal.pgen.1010651
- Brundage DM (2026). CanVAS: A Harmonized and Imputed Canine Variant Atlas. bioRxiv. doi:10.64898/2026.04.13.718238
- Nicholas, F.W., Tammen, I., & Sydney Informatics Hub. (2026). Online Mendelian Inheritance in Animals (OMIA) [dataset]. The University of Sydney. https://omia.org. doi:10.25910/2AMR-PV70 (retrieved April 2026).