AI portrait
This portrait was algorithmically built from this dog's genome: their genotype at 8 morphology loci (coat length, curl, color, ear set, body size, head shape, skull, furnishings) plus their position within the 14,478-dog atlas. The same dog always reproduces the same portrait. A different dog with different alleles gets a different portrait.
RTVB_RTVB_31258
RTVB_RTVB_31258 is a Retriever Breed Unknown from the Spatola research cohort. One of 14,478 dogs who built the atlas.
See RTVB_RTVB_31258 in the atlasRTVB_RTVB_31258 is a notable Retriever Breed Unknown - distinctive within the breed.
- Predicted large by the six body-size genes the atlas reads (IGF1, HMGA2, SMAD2, LCORL, STC2, ADAMTS17).
- Carries both copies of the FGF4 chondrodysplasia retrogene - the short-leg variant in Dachshund, Pembroke Corgi, Basset Hound.
- Smooth coat. No wire-furnishings variant at RSPO2.
The five dogs in the atlas whose genomes sit closest to RTVB_RTVB_31258's. Click any of them to keep exploring.
RTVB_RTVB_31258 sits in the Labrador Retriever cluster, with genome overlap to Golden Retriever - sister breeds nearby in the atlas.
Breed similarity from non-negative least squares against 91 breed centroids in PCA-256 space, corrected for atlas sample-size imbalance. Without correction, Goldens (22% of the atlas) leak into every dog's raw NNLS breakdown; with it, the bias falls out. Raw fractions stay in the dataset for re-derivation. Methodology.
- Labrador Retriever 56%
- Golden Retriever 44%
From the CanVAS (Spatola cohort) . Breed-page reference: Retriever Breed Unknown.
Full genotype detail click to expand
The actual allele call at each locus's representative SNP for this dog. Each gene name links to its page where you can see the per-breed frequency table and the direction of effect.
Technical details click to expand
The numbers behind the placement. Useful for researchers reproducing the math or debugging an unexpected position; not interesting to most readers.
y 5.748
z 4.516
The 3 PCs on which RTVB_RTVB_31258 scores most extreme, with the 3 highest-loading SNPs on each. Foundation for the future genome-ring visualization.
- chr30:3,320,848 loading 0.0326
- chr30:3,423,077 loading 0.0326
- chr30:3,200,238 loading 0.0321
- chr13:43,330,325 loading 0.0255
- chr17:50,562,684 loading 0.0245
- chr19:34,146,978 loading 0.0244
- chr11:28,721,751 loading 0.0412
- chr14:3,689,618 loading -0.0355
- chr11:17,928,935 loading -0.0339