Across TCGA pan-cancer cohorts, AP1M1 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated AP1M1 data layer compared with 27 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in kidney chromophobe (KICH), where higher AP1M1 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated AP1M1 expression acts as an unfavorable survival marker.
KICH and PRAD are the cancer types where AP1M1 Mutation most reproducibly stratifies survival.