Across TCGA pan-cancer cohorts, FOXB2 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated FOXB2 data layer compared with 14 for mass-spec protein.
The strongest signal is observed in head and neck squamous cell carcinoma (HNSC), where higher FOXB2 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated FOXB2 expression acts as an unfavorable survival marker.
HNSC and LUSC are the cancer types where FOXB2 Mutation most reproducibly stratifies survival.