CNP
CNP is a gene catalogued in the canine genome. Here is its canonical identity across the genomics world and, where documented, its human counterpart.
CNP as it is catalogued across the genomics world. Each link is the canonical record, so this gene composes with everything those resources know.
In humans, this gene's counterpart is CNP. That ortholog is what connects CNP to a century of human medical genetics. The dog and human proteins are 81% identical.
In people, CNP rarely tolerates loss-of-function variation (gnomAD v4.1 constraint, LOEUF 0.38), a sign it does important, dosage-sensitive work.
In people, variants in the CNP gene are reported as pathogenic in ClinVar but not yet at our 3★ expert-panel bar (criteria-provided submissions can exist without expert-panel review). The evidence is limited, not that variants here are benign.
In dogs, 11 of 266 Dog10K variants in this gene sit at a position kept conserved across 241 mammals (the exhaustive scan), candidates worth a closer look, never a diagnosis.
Dog and human evidence are symmetric here, a validated cross-species footprint. Coverage, not importance. D = 1 dog vs H = 1 human cited disease channels.
Lookup and discovery are candidate-framed research surfaces. Classification renders AVCG grades we cite; Sniff does not score variants with a model of its own.
Per-breed allele frequencies across the atlas are surfaced for the trait loci Sniff has verified a direction-of-effect for. For CNP we show the cited identity and disease associations, and we would rather show you exactly that than a frequency we cannot yet interpret honestly. See the gene catalog for trait loci with frequency views and every disease-linked gene page.
Gene identity and disease associations are grounded in OMIA (CC-BY) and the open Sniff Atlas. Full citation formats at sniff.world/cite.