Across TCGA pan-cancer cohorts, FBXO39 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated FBXO39 data layer compared with 24 for mass-spec protein.
The strongest signal is observed in prostate adenocarcinoma (PRAD), where higher FBXO39 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated FBXO39 expression acts as an unfavorable survival marker.
PRAD and UCEC are the cancer types where FBXO39 Mutation most reproducibly stratifies survival.