Across TCGA pan-cancer cohorts, MT1G Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated MT1G data layer compared with 22 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in colon adenocarcinoma (COAD), where higher MT1G Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated MT1G expression acts as an unfavorable survival marker.
COAD, LUSC, and KIRP are the cancer types where MT1G Mutation most reproducibly stratifies survival.