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Discovery / research surface

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One entry point for the whole substrate. Type a gene (human or dog), a human variant, a Dog10K position, a breed, or a human disease. A gene or variant resolves right here against the Dog10K → human disease map; a breed or a human disease opens its lens. When the answer is nothing, it always tells you why.

Human → dog is first-class. Ask "does any Dog10K dog carry a variant at this human disease position?" and you get the orthologous-position answer. We report where a variant sits, never that a dog allele is identical to a human one (that is a separate, harder claim, INV-57).
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Want the ranked landscape instead of a single lookup? See the full candidate list →

How "not found" answers

Every empty result returns exactly one reason, the first rung that failed, in order:

  1. 1Not in the disease-gene set, no human P/LP ClinVar evidence to bridge from. (not "the dog is clear")
  2. 2No one2one ortholog, a human disease gene, but the dog ortholog is unmapped or one-to-many; the bridge requires one2one (INV-56).
  3. 3Nothing cleared the stack, anchored, but no Dog10K variant in the gene passed the evidence gate. (gene-level; the per-variant rung, bare position vs mechanism mismatch, is the next data drop)
  4. Cleared, a Dog10K variant sits at a human disease position and cleared the stack. A candidate, never a confirmed model.

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Sources: Dog10K (Meadows 2023), Ensembl Compara + OrthoDB + OMA orthology, ClinVar (Landrum 2018), gnomAD (Karczewski 2020), MONDO/OMIM, Evo 2 (Arc 2026). Gene-level (INV-57). Candidates are computational hypotheses; confirmation is DNA + phenotype, in the lab.