Across TCGA pan-cancer cohorts, FOXI3 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated FOXI3 data layer compared with 19 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in kidney chromophobe (KICH), where higher FOXI3 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated FOXI3 expression acts as an unfavorable survival marker.
KICH and SKCM are the cancer types where FOXI3 Mutation most reproducibly stratifies survival.