Across TCGA pan-cancer cohorts, METTL24 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated METTL24 data layer compared with 24 for mass-spec protein.
The strongest signal is observed in stomach adenocarcinoma (STAD), where higher METTL24 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated METTL24 expression acts as an unfavorable survival marker, although some lineages such as SKCM show a favorable association.
STAD, COAD, and SKCM are the cancer types where METTL24 Mutation most reproducibly stratifies survival.