Across TCGA pan-cancer cohorts, MOGAT3 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated MOGAT3 data layer compared with 21 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher MOGAT3 Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated MOGAT3 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
UCEC and PRAD are the cancer types where MOGAT3 Mutation most reproducibly stratifies survival.