Across TCGA pan-cancer cohorts, RPL22 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated RPL22 data layer compared with 26 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher RPL22 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated RPL22 expression acts as an unfavorable survival marker.
OV, COAD, and UCEC are the cancer types where RPL22 Mutation most reproducibly stratifies survival.