Across TCGA pan-cancer cohorts, ATPSCKMT Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated ATPSCKMT data layer compared with 26 for mass-spec protein and 2 for mass-spec protein.
The strongest signal is observed in bladder urothelial carcinoma (BLCA), where higher ATPSCKMT Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated ATPSCKMT expression acts as an unfavorable survival marker.
BLCA, UCEC, and COAD are the cancer types where ATPSCKMT Mutation most reproducibly stratifies survival.