Across TCGA pan-cancer cohorts, MT1A Mutation is linked to patient survival in 1 of 34 cancer types, making it a survival-associated MT1A data layer compared with 22 for mass-spec protein and 3 for mass-spec protein.
The strongest signal is observed in prostate adenocarcinoma (PRAD), where higher MT1A Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated MT1A expression acts as an unfavorable survival marker.
PRAD are the cancer types where MT1A Mutation most reproducibly stratifies survival.