Across TCGA pan-cancer cohorts, RALY Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated RALY data layer compared with 23 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in breast invasive carcinoma (BRCA), where higher RALY Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated RALY expression acts as an unfavorable survival marker.
BRCA, PRAD, and UCEC are the cancer types where RALY Mutation most reproducibly stratifies survival.