Across TCGA pan-cancer cohorts, ACOT1 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated ACOT1 data layer compared with 28 for mass-spec protein and 2 for mass-spec protein.
The strongest signal is observed in kidney chromophobe (KICH), where higher ACOT1 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated ACOT1 expression acts as an unfavorable survival marker.
KICH and COAD are the cancer types where ACOT1 Mutation most reproducibly stratifies survival.