Dogue De Bordeaux
9 Dogue De Bordeauxs in the atlas. Every number on this page has a source.
9 Dogue De Bordeauxs in the Sniff Atlas. Population-genetic snapshot, Mendelian carrier frequencies from Donner 2023, and the data substrate's release version, sample sizes, and evidence tier on every claim.
In the atlas, the Dogue De Bordeaux clusters consistently as Dogue De Bordeaux (100% of the 9 dogs here). Genetic diversity is high (mean heterozygosity 0.3268), reflecting either a mixed-breed cluster or breeds with broad genetic backgrounds. At the trait loci, STC2 runs lower than average (20% here vs 74%); FGF5 runs lower than average (17% here vs 64%). Dogs here sit in a relatively sparse region of the atlas, fewer close neighbors than typical.
Mean heterozygosity is 0.327, notably high, indicates broad genetic background. High breed predictability score (1.03), individual dogs of this breed reliably cluster together genetically. Only 9 dogs of this breed in the atlas, every individual contributes outsized weight to the breed's computed profile.
Closest genetic neighbors in the atlas: French Bulldog, Boston Terrier, Mastiff, Cane Corso, and Staffordshire Bull Terrier.
What the genome says about Dogue De Bordeaux
Computed from the 18,477 research dogs in the Atlas.
- French Bulldog11.62
- Boston Terrier14.67
- Mastiff16.28
- Cane Corso17.75
- Staffordshire Bull Terrier18.35
Frequency of the alternate allele in this breed at each locus's representative SNP.
| IGF1 | 33% |
| HMGA2 | 83% |
| SMAD2 | 78% |
| LCORL | 83% |
| STC2 | 20% |
| ADAMTS17 | – |
| FGF4·CFA18 | 100% |
| FGF4·CFA12 | 100% |
| RSPO2 | 43% |
| FGF5 | 17% |
| KRT71 | 94% |
| MC1R | 78% |
| MSRB3 | – |
| BMP3 | – |
| SMOC2 | 78% |
What does the genome say about how a Dogue De Bordeaux looks?
Dogue De Bordeauxs 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.
Size and build
IGF1 sits at 33% 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.
HMGA2 sits at 83%. HMGA2 is a chromosome-10 size locus that acts together with IGF1, and intermediate frequencies reflect partial commitment to the dominant size variant.
SMAD2 sits at 78% at the chromosome-7 height locus.
LCORL sits at 83% at the NCAPG/LCORL height locus on chromosome 3.
STC2 is at 20%, leaving the growth-axis signal to other loci.
ADAMTS17 is at 0%, the lower-frequency allele in this breed.
Leg length
The FGF4 retrogene on chromosome 18 is near-fixed in this breed at 100%. This is the leg-length variant. The breed is fully committed to the long-legged form rather than the short-legged Corgi-and-Dachshund body plan.
The FGF4 retrogene on chromosome 12 is near-fixed at 100%, the chondrodystrophic variant associated with intervertebral disc disease risk in breeds that carry it.
Coat type, length, and color
RSPO2 sits at 43% 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.
FGF5 is at 17% for the long-coat variant, which keeps the breed in the short-coated form.
KRT71 is near-fixed at 94% 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.
MC1R sits at 78% at the representative SNP. MC1R controls the switch between red-to-gold pigment and black-to-brown pigment, with the e/e homozygous genotype producing the gold-to-red spectrum. Substrate frequencies at this SNP depend on the array's polarity, so visible coat color in the breed is a more reliable indicator than this single number.
Ears
MSRB3 is at 0% for the drop-ear allele, keeping the breed's ears upright and prick.
Skull shape
BMP3 is at 0%, keeping the breed in the dolichocephalic, long-headed form.
SMOC2 sits at 78%, contributing to the breed's moderate head shape.
What genetic diseases do Dogue De Bordeauxs carry?
From a panel of 250 Mendelian-disease variants screened in 1,054,293 dogs (Donner et al. 2023), Dogue De Bordeauxs carry 4 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.
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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- Donner J, Anderson H, Davison S, et al. (2023). Frequency and distribution of 152 genetic disease variants in over 1,000,000 mixed-breed and purebred dogs. PLOS Genetics 19(2):e1010651. doi:10.1371/journal.pgen.1010651
- Brundage J, et al. (2026). CanVAS: a harmonized 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).