Across TCGA pan-cancer cohorts, MRPL32 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated MRPL32 data layer compared with 27 for mass-spec protein and 3 for mass-spec protein.
The strongest signal is observed in breast invasive carcinoma (BRCA), where higher MRPL32 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated MRPL32 expression acts as an unfavorable survival marker.
BRCA, SARC, and UCEC are the cancer types where MRPL32 Mutation most reproducibly stratifies survival.