Across TCGA pan-cancer cohorts, SPDYE2 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated SPDYE2 data layer compared with 24 for mass-spec protein.
The strongest signal is observed in prostate adenocarcinoma (PRAD), where higher SPDYE2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SPDYE2 expression acts as an unfavorable survival marker.
PRAD and UCEC are the cancer types where SPDYE2 Mutation most reproducibly stratifies survival.