Across TCGA pan-cancer cohorts, BRI3 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated BRI3 data layer compared with 27 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in mesothelioma (MESO), where higher BRI3 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated BRI3 expression acts as an unfavorable survival marker.
MESO and HNSC are the cancer types where BRI3 Mutation most reproducibly stratifies survival.