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Bulldog

Bulldog
Photo: Ultimoribelle / CC BY-SA 4.0 · Wikimedia

38 Bulldogs in the atlas. Every number on this page has a source.

Population-genetic snapshot of Bulldogs in the Sniff Atlas, source-graded Mendelian carrier frequencies from Donner 2023, and nutrition guidance tied to the genetic findings above.

Also known as British Bulldog and English Bulldog.

The plain version

Bulldogs have a moderately diverse genetic background. They are medium-sized dogs, usually weighing around 53 pounds, and typically live about 8 to 9 years. No specific health concerns showed up in genetic screenings for this breed, but it’s always a good idea to consult your vet or consider testing to keep your dog at its best.

What the atlas says about Bulldog

In the atlas, the Bulldog clusters consistently as Bulldog (100% of the 38 dogs here). At the trait loci, SMOC2 runs lower than average (32% here vs 75%); HMGA2 runs lower than average (22% here vs 56%). Dogs here sit in a relatively sparse region of the atlas, fewer close neighbors than typical.

Median lifespan is 8.6 years, about 3.2 years shorter than a typical dog of 24.0 kg, one of the larger gaps in the atlas.

Genetic dimensions · CanVAS atlas

What the genome says about Bulldog

Computed from the 18,477 research dogs in the Atlas.

Dogs in the Atlas
38Founders
24 from Hayward2016, 9 from Spatola, 3 from JenkinsWGS
Genetic diversity
0.29Moderate
Mean heterozygosity across the breed. Ranks 29th most genetically tight of 107 ranked breeds.
What does genetic diversity mean?

How varied a breed's gene pool is — the share of gene spots where a typical dog of the breed carries two different versions rather than two identical ones.

How to read it: Higher = more diverse. Among well-sampled breeds it ranges roughly 0.22 (least diverse) to 0.33 (most diverse).

Diversity is a strength, not a verdict on any individual dog. Lower diversity means it's worth paying attention to recessive-risk testing — not that a dog is doomed.

Cluster structure
Splits into two genetic sub-populations
Intra-breed RMS distance: 49.88 · likely working/show-line, regional, or kennel lineage split.
What does within-breed variation mean?

How much individual dogs within the breed differ from each other genetically.

How to read it: Higher = more internal variety among individuals of the breed.

Sensitive to how many dogs of the breed we've sampled.

Related breeds
Gave rise to
In the Non-Sporting group
Explore the full lineage map →
VBO foundation stock (breeding records) · AKC breed group
Relatedness is documented lineage + kennel family. Genetic-ancestry distance measures diversity, not kinship, so it isn't used here.
How long they live
9.8years (life expectancy)
95% CI 9.7–10 · VetCompass, McMillan 2024, n=11,065. source
What does typical lifespan mean?

The median age dogs of the breed tend to reach.

How to read it: Higher = longer-lived. Compare to longevity-for-size to see whether it's just a size effect.

Drawn from population lifespan records; individual dogs vary widely with care, genetics, and luck.

Trait genetics
Allele frequencies at named morphology loci

Frequency of the alternate allele in this breed at each locus's representative SNP.

Body size
IGF165%
HMGA222%
SMAD290%
LCORL80%
STC267%
ADAMTS1750%
Leg length
FGF4·CFA1876%
FGF4·CFA1293%
Coat
RSPO276%
FGF561%
KRT7192%
MC1R90%
Ear set
MSRB386%
Skull shape
BMP376%
SMOC232%
n = 38 dogs · moderate confidence · CanVAS (Brundage 2026) · Sniff Atlas
Names & origins

Other names

The Bulldog is also recorded as British Bulldog and English Bulldog.

Identified as Bulldog (VBO:0200258) in the Vertebrate Breed Ontology (Mullen et al. 2025, CC-BY 4.0) · registry IDs FCI 149 · iDog 58 · VeNom 13759.

What you see when you look at a Bulldog

What does the genome say about how a Bulldog looks?

Bulldogs look the way they do because of a small set of fixed and near-fixed morphology genes that, taken together, define the visible breed. Each translation below pairs the gene with the trait an owner actually sees, the breed's allele frequency at that locus, and a one-clause causal phrase.

Where the breed-defining genes act, mapped on a generic dog-body key — and how fixed each marker is in the Bulldog. The figure is the most-settled marker we read in that region; the full per-locus panel is below. (The silhouette is a shared anatomical guide, not this breed's outline.)

Body sizeSMAD2 · 90%Skull shapeBMP3 · 76%EarsMSRB3 · 86%Leg lengthFGF4 CFA12 · 93%Coat & colorKRT71 · 92%
CanVAS trait-locus panel (Brundage 2026)
15 morphology markers read across 5 regions. Allele frequency = how fixed a marker is in this breed, not whether your dog carries it.

Size and build

IGF1 sits at 65% for the small-body allele. IGF1 is the gene that sets dog body size from Chihuahua to Great Dane. Intermediate frequencies typically keep a breed in the mid-sized range rather than tipping toward the larger working forms.

IGF1what this gene does

IGF1 is a gene that plays a key role in determining a dog's body size. It influences how much a dog grows, affecting overall stature.

For your dog: Knowing about IGF1 gives you insight into your dog's size traits, but it’s just one part of the bigger picture when it comes to their health and care.

Full IGF1 gene page →

HMGA2 is at 22%, leaving most of the size signal to other loci in the panel.

HMGA2what this gene does

HMGA2 is a gene that influences body size in dogs, helping determine how big or small a dog grows.

For your dog: Knowing about HMGA2 helps you appreciate the genetic factors behind your dog's size, but it doesn't signal any health issues.

Full HMGA2 gene page →

SMAD2 is near-fixed at 90%, a chromosome-7 height locus differentiating small from giant breeds.

SMAD2what this gene does

SMAD2 is a gene involved in regulating body size by influencing how cells grow and develop.

For your dog: Knowing about SMAD2 helps understand your dog's size traits but isn't linked to health issues; no immediate action needed.

Full SMAD2 gene page →

LCORL sits at 80% at the NCAPG/LCORL height locus on chromosome 3.

LCORLwhat this gene does

LCORL is a gene that influences body size in dogs. It helps determine how big or small a dog might grow.

For your dog: Knowing about LCORL helps you appreciate the genetic factors behind your dog's size, but it’s just one piece of the bigger picture when it comes to health and care.

Full LCORL gene page →

STC2 sits at 67%.

ADAMTS17 sits at 50%. ADAMTS17 is a body-size locus also linked to lens disorders.

ADAMTS17what this gene does

ADAMTS17 is a gene that influences body size and also plays a role in certain eye conditions. It affects the structure of tissues in the eye and elsewhere in the body.

For your dog: If your dog belongs to a breed known to carry ADAMTS17 variants, it’s worth discussing genetic testing and eye exams with your vet to stay ahead of potential issues.

Full ADAMTS17 gene page →

Leg length

The FGF4 retrogene on chromosome 18 sits at 76%. This is the leg-length variant. The intermediate frequency means some dogs in this breed carry the short-legged allele and some do not.

The FGF4 retrogene on chromosome 12 is near-fixed at 93%, the chondrodystrophic variant associated with intervertebral disc disease risk in breeds that carry it.

Coat type, length, and color

RSPO2 sits at 76% for the furnishings variant. Furnishings (the eyebrow-and-mustache pattern seen in Schnauzers and Wheaten Terriers) vary across the population at this intermediate frequency, and visible expression depends on the specific allele combination each dog carries.

RSPO2what this gene does

RSPO2 influences the texture and appearance of a dog's coat, particularly the presence of 'furnishings' like mustaches and eyebrows. It helps determine whether a dog has that distinctive wiry or textured look.

For your dog: If your dog has those wiry eyebrows or a mustache, RSPO2 is part of the reason—no health worries, just a coat feature worth knowing about.

Full RSPO2 gene page →

FGF5 sits at 61% for the long-coat variant. Coat length is influenced by other loci as well, so intermediate FGF5 frequencies do not always correspond to intermediate visible coat lengths.

FGF5what this gene does

FGF5 is a gene that influences the length of a dog's coat. It acts like a natural switch, telling hair follicles when to stop growing longer fur.

For your dog: If your dog has a notably long or short coat, FGF5 is likely part of the reason—no action needed, but it’s a neat genetic detail to know.

Full FGF5 gene page →

KRT71 is near-fixed at 92% for the wavy/curly variant. Coat curl phenotype varies across breeds at this fixation depending on modifier loci, and visible expression is not always curled even when the locus is fixed.

KRT71what this gene does

KRT71 is a gene that influences the curliness of a dog's coat. It helps determine whether a dog's fur is straight or has a distinctive curl.

For your dog: If your dog has a curly coat, KRT71 is likely part of the reason; it’s a natural variation, not a health concern.

Full KRT71 gene page →

MC1R is at 90% at the representative SNP. MC1R controls the switch between red-to-gold and black-to-brown pigment, with the e/e homozygous genotype producing the gold-to-red spectrum by blocking eumelanin (black and brown pigment).

MC1Rwhat this gene does

MC1R is a gene that influences coat color in dogs, affecting how pigments are produced in the fur.

For your dog: Knowing about MC1R gives insight into your dog's coat color but doesn't relate to health issues.

Full MC1R gene page →

Ears

MSRB3 is at 86% for the drop-ear allele, the genetic basis of the breed's signature dropped ear set.

MSRB3what this gene does

MSRB3 is a gene involved in the development of ear shape and structure in dogs.

For your dog: Understanding MSRB3 helps explain why your dog's ears look the way they do, but it isn't linked to any health issues.

Full MSRB3 gene page →

Skull shape

BMP3 sits at 76%, contributing to the breed's moderate, mesaticephalic head shape rather than the extreme brachycephalic form.

BMP3what this gene does

BMP3 is a gene that influences the shape of a dog's skull, particularly contributing to a shorter, broader head shape known as brachycephaly.

For your dog: If your dog has a broad, short skull, it's worth discussing with your vet how this might impact their health, even though BMP3 isn't directly tied to illness.

Full BMP3 gene page →

SMOC2 sits at 32%, contributing to the breed's moderate head shape.

SMOC2what this gene does

SMOC2 influences the shape of a dog's skull, particularly affecting how flat or short the face appears.

For your dog: If your dog has a short nose, it's worth discussing with your vet how this trait might impact their health over time.

Full SMOC2 gene page →
Mendelian-disease genetics

What genetic diseases do Bulldogs carry?

From a panel of 250 Mendelian-disease variants screened in 1,054,293 dogs (Donner et al. 2023), Bulldogs carry 19 of them at observable frequency. Carrier frequency 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.

Cystinuria Type I-B (SLC7A9 p.A217T)
Autosomal recessive (Incomplete penetrance)
high 55.5%
n = 4,816 dogs · 2 variants tested · OMIA:001880-9615 · omia.org →
SLC7A9what this gene does

SLC7A9 is a gene that helps transport certain amino acids in the kidneys. It plays a role in how the body handles cystine, an amino acid that can form crystals.

For your dog: If your dog is a carrier, it’s worth discussing with your vet to monitor urinary health and catch any issues early.

high 39.4%
n = 4,816 dogs · 3 variants tested · OMIA:000256-9615 · omia.org →
SLC3A1what this gene does

SLC3A1 is a gene that helps transport certain amino acids in the kidneys. It plays a key role in preventing the buildup of cystine, which can form stones.

For your dog: If your dog is from a breed known to carry SLC3A1 variants, it’s worth discussing cystinuria risks with your vet, especially if urinary issues arise.

Hyperuricosuria (HUU)
Autosomal recessive
moderate 17.9%
n = 4,816 dogs · 1 variant tested · OMIA:001033-9615 · omia.org →
SLC2A9what this gene does

SLC2A9 is a gene that helps regulate uric acid levels in a dog's body. It plays a role in how the kidneys handle this substance.

For your dog: If your dog is one of the breeds known to carry this gene variant, it’s worth discussing with your vet to understand any potential urinary health concerns.

n = 4,816 dogs · 1 variant tested · OMIA:001444-9615 · omia.org →
BEST1what this gene does

BEST1 is a gene that helps maintain the health of the retina, the light-sensitive layer at the back of the eye. It plays a role in keeping the cells in the retina functioning properly.

For your dog: If your dog is from a breed known to carry BEST1 variants, it’s worth discussing retinal health with your vet, especially if you notice any vision changes.

Degenerative Myelopathy (DM)
Autosomal recessive (Incomplete penetrance)
moderate 12.7%
n = 4,816 dogs · 1 variant tested · OMIA:000263-9615 · omia.org →
SOD1what this gene does

SOD1 is a gene that helps protect cells from damage caused by harmful molecules called free radicals.

For your dog: If your dog is a carrier of SOD1 variants, it's worth discussing with your vet, but remember carrier status doesn't mean your dog will get the disease.

n = 4,803 dogs · 1 variant tested · OMIA:000157-9615 · omia.org →
FGF4what this gene does

FGF4 influences leg length by affecting bone growth, leading to shorter legs in certain breeds.

For your dog: If your dog is from a breed known to carry this gene, it's worth discussing spinal health with your vet, but being a carrier doesn’t guarantee problems.

Factor VII Deficiency
Autosomal recessive
low 0.58%
n = 4,815 dogs · 1 variant tested · OMIA:000361-9615 · omia.org →
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.

Cone-Rod Dystrophy (cord1-PRA/crd4)
Autosomal recessive (Incomplete penetrance)
low 0.20%
n = 4,808 dogs · 1 variant tested · OMIA:001432-9615 · omia.org →
RPGRIP1what this gene does

RPGRIP1 is a gene involved in the function of photoreceptor cells in the eye, which help dogs see in different light conditions.

For your dog: If your dog belongs to a breed known to carry RPGRIP1 mutations, it’s worth discussing with your vet to understand the risks and monitor eye health.

n = 4,816 dogs · 2 variants tested · OMIA:000162-9615 · omia.org →
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.

n = 4,816 dogs · 1 variant tested · OMIA:001980-9615 · omia.org →
n = 4,816 dogs · 1 variant tested · OMIA:001402-9615 · omia.org →
ABCB1what this gene does

ABCB1 is a gene that helps control how certain drugs are processed and cleared from a dog's body.

For your dog: If your dog is from a breed that carries this gene variant, ask your vet about medication sensitivities before giving any new drugs.

n = 4,815 dogs · 1 variant tested · OMIA:001503-9615 · omia.org →
ARSGwhat this gene does

ARSG is a gene that helps break down certain molecules in the body, keeping cells healthy.

For your dog: If your dog is from a breed known to carry ARSG mutations, it's worth discussing genetic testing with your vet to understand potential health risks.

n = 4,816 dogs · 2 variants tested · OMIA:000341-9615 · omia.org →
n = 4,816 dogs · 2 variants tested · OMIA:002120-9615 · omia.org →
NDRG1what this gene does

NDRG1 is a gene involved in nerve cell function and maintenance, helping keep the nervous system working properly.

For your dog: If your dog is from a breed known to carry NDRG1 variants, it’s worth discussing with your vet, especially if you notice any mobility issues.

Hypocatalasia
Autosomal recessive
low <0.1%
n = 4,815 dogs · 1 variant tested · OMIA:001138-9615 · omia.org →
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.

Collie Eye Anomaly (CEA)
Autosomal recessive
low <0.1%
n = 4,816 dogs · 1 variant tested · OMIA:000218-9615 · omia.org →
NHEJ1what this gene does

NHEJ1 is a gene involved in repairing breaks in DNA, helping maintain the integrity of genetic information in cells.

For your dog: If your dog belongs to one of the breeds known to carry this gene variant, it's worth discussing testing with your vet to understand any potential eye health risks.

Shar-Pei Autoinflammatory Disease (SPAID)
Autosomal dominant (Incomplete penetrance)
low <0.1%
n = 4,816 dogs · 1 variant tested · OMIA:001561-9615 · omia.org →
MTBPwhat this gene does

MTBP is a gene involved in regulating inflammation in the body. It helps control how the immune system responds to triggers.

For your dog: If your dog is from a breed known to carry MTBP variants, it's worth discussing with your vet whether genetic testing or monitoring for inflammation-related issues makes sense.

Source: Donner J et al. 2023. Genetic prevalence and clinical relevance of canine Mendelian disease variants in over one million dogs. PLOS Genetics 19(2):e1010651 · Evidence: Limited (DTC ascertainment, tag-SNP proxy) · Confounding MEDIUM · License CC-BY-4.0 · Phene IDs from OMIA (Sydney School of Veterinary Science, The University of Sydney; DOI 10.25910/2AMR-PV70).
Sample size in this breed: 4,816 dogs from the Donner 2023 cohort.

Which Mendelian variants matter most for Bulldogs?

No Mendelian variants reached observable carrier frequency in the Bulldog cohort tested (Donner 2023). This is not the same as saying Bulldogs carry no recessive disease variants. It means the atlas sample (n=38) is too small to detect variants below roughly 10% carrier frequency, and the breed’s population bottleneck (genetic diversity rank 29 of 107) may have fixed some variants and purged others. The substrate cannot tell us which.

What we can see is the morphology. Bulldogs are fixed for the chondrodystrophy variants FGF4 retrogene at 76% (CFA18) and 93% (CFA12). The breed standard calls for shortened limbs and a massive skull, which maps onto SMAD2 at 90% and BMP3 at 76%. These variants define the Bulldog silhouette, but they also carry real health costs: IVDD risk, airway restriction, and heat intolerance are direct consequences. But they set the constraints for everything below: heat tolerance, breathing, joint loading, and lifespan.

What should I feed a Bulldog?

Bulldogs can’t pant efficiently, which means heat-of-the-day exercise is dangerous and meal timing matters more than it does for most breeds. The FGF4 retrogene variants (76% at CFA18, 93% at CFA12) are fixed at high frequency in Bulldogs and are associated with chondrodystrophy, shortened limbs, and elevated intervertebral disc disease (IVDD) risk. Shortened limbs carry concentrated joint loading per stride. A Bulldog’s spine and hips are under constant mechanical stress that taller breeds distribute across longer bones.

Puppy feeding is where the joint trajectory gets set. A large-breed puppy formula with controlled calcium (0.8% to 1.2% on a dry-matter basis) and a calcium-to-phosphorus ratio between 1.1:1 and 2:1 is the foundation (NRC 2006). Bulldogs grow from 2 to 3 pounds at birth to 40 to 50 pounds at adulthood. That growth rate is fast enough that overfeeding calcium, even with a “large-breed” label, can accelerate joint disease. Feed to a growth chart, not to appetite. A Bulldog puppy should be lean enough that you feel the ribs without pressing.

Adult weight management is the other half. Bulldogs have a low spontaneous activity level compared to longer-limbed breeds, and owners often feed to the dog’s apparent appetite rather than to energy expenditure. Excess weight compounds the joint loading problem and is a documented concern in the breed (Bulldogclub.org health committee recommendations). Aim for a body condition score of 4 to 5 out of 9 (AAFCO standard). A calorie-controlled adult formula fed in measured portions, rather than free-feeding, is the generally accepted best practice for weight-prone brachycephalic breeds.

Heatstroke risk shifts meal timing. Bulldogs cannot thermoregulate efficiently, especially during exercise or in warm weather. Heavy meals during heat-of-the-day can impair panting and cooling. Feed the main meal in the cool morning and evening hours, with light treats only during midday. This is one of the few breed-specific feeding rules that is non-negotiable.

Grain-free diets carry unclear risk for this breed. The FDA’s 2018 advisory and Adin et al. 2019 (JVIM) flagged dilated cardiomyopathy in Goldens and some other breeds fed certain grain-free, pulse-heavy formulations. Bulldogs are not named in the FDA dataset with high frequency. The conservative default is still a grain-inclusive, taurine-supplemented adult formulation, but the evidence is less compelling for this breed than for Goldens or Dalmatians. Either approach is defensible; grain-inclusive is simply the safer assumption given the broader data.

What we don’t know

The atlas sample of 38 Bulldogs is below the threshold where Mendelian screening has statistical power. Carrier frequencies below roughly 10% will not surface, and the breed’s tight founder structure (24 dogs from Hayward 2016, 9 from Spatola, 3 from Jenkins, 1 from Shannon) means low-frequency recessives may be fixed or absent by chance rather than by health. We cannot say whether Bulldogs are truly free of recessive disease variants or whether the sample is simply too small to find them.

The breed’s shortened lifespan (atlas median 8.6 years) is consistent with the severe morphology, shortened limbs, compact skull, flat face, and small nasal passages. We do not know how much of the lifespan gap is unavoidable given the breed standard and how much is modifiable through selection, weight management, and early intervention for airway obstruction and heat intolerance. The honest summary is that the breed’s conformation sets hard limits that we have not yet parsed from modifiable risk.

Frequently asked questions about Bulldogs

Why do Bulldogs have such short lifespans? The atlas median is 8.6 years (Donner 2023), well below the all-breed median. The shortened limbs (FGF4 retrogene at 76-93%), compact skull (BMP3 at 76%), and flat face that define the breed standard also constrain heat tolerance, airway capacity, and joint geometry. These are the breed, not fixable through diet alone.

Are Bulldogs prone to hip dysplasia? Yes. The breed’s low back-to-hip ratio and concentrated joint loading create a geometric predisposition. The OFA has not published a breed-specific prevalence figure for Bulldogs. Weight management and controlled growth in puppyhood are the primary preventions.

Can I overfeed a Bulldog puppy? Yes, and it matters. Overfeeding calcium and calories in large-breed puppies accelerates joint disease. Use a large-breed puppy formula and feed to a growth chart, not to appetite. A lean puppy at 12 weeks will thank you at age five.

Should I feed my Bulldog grain-free? Not unless your vet identifies a specific protein allergy. The FDA’s cardiac-risk advisory did not flag Bulldogs as a primary-affected breed, but grain-inclusive formulations remain the conservative default. Ensure the food is taurine-supplemented either way.

What time of day should I feed my Bulldog? Early morning and evening, when it is cool. Bulldogs can’t pant efficiently, and digestion during heat-of-the-day can impair cooling. This is non-negotiable in summer and warm climates.

Is my Bulldog’s breathing normal? Not necessarily. Many Bulldogs have airway obstruction (brachycephalic obstructive airway syndrome, BOAS) that owners interpret as normal snoring. If your Bulldog struggles to cool down after light exercise, has noisy breathing at rest, or seems to tire quickly, ask your vet about airway assessment. Early surgical intervention for BOAS is associated with improved respiratory function in affected dogs (Poncet et al. 2006, JSAP 47:315-323).

Do Bulldogs need special joint supplements? Peer-reviewed evidence supporting glucosamine or chondroitin as prevention for hip dysplasia is lacking across breeds (Innes et al. 2003, JSAP 44:400). Weight management and controlled growth are proven. Supplements are an optional add-on, not a substitute.

Should I get a DNA test for my Bulldog? A whole-genome sequence would be informative (the atlas has only 38 dogs), but a commercial panel would not flag Mendelian variants at the carrier frequency in the current substrate. If you breed, a sequence is worth considering for future population management. For a pet, it is optional.

A gift to human medicine

Bulldogs are a natural model for human disease

Because the same genes cause the same conditions across species, the inherited conditions documented in Bulldogs help researchers understand, and work toward treating, the human diseases they model. This is the dog advancing human medicine. The breed models the human disease; it does not have it, and this is not a prediction for your dog.

Human equivalents via OMIA → Mondo / OMIM. Model-of, not identity.
Documented in OMIA

Every condition recorded in the Bulldog

Beyond the testable carriers above, OMIA's literature catalogue records 4 genetic conditions in the Bulldog, 3 of which have a known human equivalent. This is the documented landscape across all Bulldogs ever studied, not a prediction for any one dog.

Online Mendelian Inheritance in Animals (OMIA); Nicholas, Tammen & Sydney Informatics Hub, DOI 10.25910/2AMR-PV70
Documented in the breed's literature is not carrier status and not a forecast for an individual dog. Human equivalents are mapped via Mondo/OMIM. Carrier frequencies (above) are the separately-measured testable subset (Donner 2023).
The data behind this page

Where every number on this page came from.

This page draws on three primary data sources. Carrier frequencies for the Mendelian section come from Donner et al. 2023 (CC-BY-4.0). We grade these data at evidence Limited because the cohort is a direct-to-consumer ascertainment, which biases toward owners who chose to test their dogs. The panel also uses tag-SNP proxies for some variants rather than direct causal-variant assays. Limited is a study-design grade, not a quality grade: the Donner cohort is the largest open canine-genotype dataset in existence and we are grateful for it. We rate the confounding MEDIUM.

Population-genetic dimensions (heterozygosity, intra-breed PCA distance, nearest neighbors, trait-locus frequencies) come from CanVAS (Brundage 2026), harmonized through the Sniff Atlas. The exact release date and verification commit are pinned at the bottom of the page so a researcher can trace a number back to a specific snapshot. The disease-gene-variant graph comes from OMIA (Online Mendelian Inheritance in Animals; Nicholas, Tammen, and the Sydney Informatics Hub at the Sydney School of Veterinary Science, The University of Sydney; retrieved April 2026, DOI 10.25910/2AMR-PV70).

What this page does not yet have. Inheritance modes and per-disease penetrance evidence from Donner 2023 are now in the structured data for every variant the panel covers. Mondo, OMIM, Ensembl, and HGNC cross-references on gene pages remain pending, they arrive in December 2026 alongside the imputed 9.67M-variant CanVAS dataset via the OMIA SQL dump absorption. Until then, gene IDs carry NCBI Gene and OMIA phene URLs only; the wider human-homolog and disease-ontology cross-reference set fills in with that release.

How to cite this page. The computed dimensions on this page are derived from the open Sniff Atlas v1.0.1 (Gehring 2026, doi:10.5281/zenodo.20566358, CC-BY 4.0). Full citation formats including BibTeX, RIS, and CITATION.cff at sniff.world/cite.

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References
  1. 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
  2. Brundage J, et al. (2026). CanVAS: a harmonized canine variant atlas. bioRxiv. doi:10.64898/2026.04.13.718238
  3. 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).
Last updated
Sources: CanVAS (Brundage 2026) · Donner 2023 · OMIA