Across TCGA pan-cancer cohorts, ZNF726 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated ZNF726 data layer compared with 28 for mass-spec protein.
The strongest signal is observed in rectum adenocarcinoma (READ), where higher ZNF726 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated ZNF726 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
READ, COAD, and UCEC are the cancer types where ZNF726 Mutation most reproducibly stratifies survival.