Across TCGA pan-cancer cohorts, REXO2 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated REXO2 data layer compared with 26 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in skin cutaneous melanoma (SKCM), where higher REXO2 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated REXO2 expression acts as an unfavorable survival marker.
SKCM and PRAD are the cancer types where REXO2 Mutation most reproducibly stratifies survival.