Across TCGA pan-cancer cohorts, XAGE3 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated XAGE3 data layer compared with 19 for mass-spec protein.
The strongest signal is observed in stomach adenocarcinoma (STAD), where higher XAGE3 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated XAGE3 expression acts as an unfavorable survival marker.
STAD, LUSC, and SKCM are the cancer types where XAGE3 Mutation most reproducibly stratifies survival.