Across TCGA pan-cancer cohorts, MOGAT2 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated MOGAT2 data layer compared with 25 for mass-spec protein.
The strongest signal is observed in uterine carcinosarcoma (UCS), where higher MOGAT2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated MOGAT2 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
UCS, UCEC, and PRAD are the cancer types where MOGAT2 Mutation most reproducibly stratifies survival.