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Cancer-driver node · fused signature

PTEN

Every register Sniff holds about PTEN, in one place, each strand cited to its source. This is a gene-level, model-of view of somatic cohort frequencies and human evidence, never a germline carrier status for an individual dog and never a per-dog prediction.

Somatic driver in canine cancer

The fraction of sequenced tumors somatically altered in PTEN, per cancer, from peer-reviewed cohorts. A cohort rate, not an individual-dog risk. Each cancer carries its cross-species concordance: whether the dog and human agree on this driver (commensurability-gated, INV-81).

Translational evidence balance
dog-ahead (unaudited) · +0.333

The dog side carries more cited disease evidence. This is unaudited: it can mean the dog literature is genuinely ahead, or that our human ingestion is incomplete (the HEXA class). It is not a target until that is ruled out. Coverage, not importance. D = 2 dog vs H = 1 human cited disease channels.

Human constraint
LOEUF 0.685
less constrained · gnomAD v4.1
Germline (human)
14
ClinVar 3-star syndromes · germline, not somatic
Dog↔human ortholog
high
1 methods · 100% identity

Germline hereditary-cancer syndromes (human)

GERMLINE variants in PTEN that cause human hereditary-cancer syndromes (ClinVar, 3-star expert-reviewed). This is a separate register from the somatic tumor drivers above, the same gene in two distinct biologies (INV-65). Each links to its Monarch/Mondo record.