Across TCGA pan-cancer cohorts, MT2A Mutation is linked to patient survival in 1 of 34 cancer types, making it a survival-associated MT2A data layer compared with 24 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in prostate adenocarcinoma (PRAD), where higher MT2A Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated MT2A expression acts as an unfavorable survival marker.
PRAD are the cancer types where MT2A Mutation most reproducibly stratifies survival.