Across TCGA pan-cancer cohorts, KRTAP5-3 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated KRTAP5-3 data layer compared with 12 for mass-spec protein.
The strongest signal is observed in stomach adenocarcinoma (STAD), where higher KRTAP5-3 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated KRTAP5-3 expression acts as an unfavorable survival marker.
STAD, LUSC, and LUAD are the cancer types where KRTAP5-3 Mutation most reproducibly stratifies survival.