Across TCGA pan-cancer cohorts, MAGOH Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated MAGOH data layer compared with 27 for mass-spec protein and 2 for mass-spec protein.
The strongest signal is observed in skin cutaneous melanoma (SKCM), where higher MAGOH Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated MAGOH expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
SKCM, SCLC, and UCEC are the cancer types where MAGOH Mutation most reproducibly stratifies survival.