Across TCGA pan-cancer cohorts, FRZB Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated FRZB data layer compared with 21 for mass-spec protein and 3 for mass-spec protein.
The strongest signal is observed in head and neck squamous cell carcinoma (HNSC), where higher FRZB Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated FRZB expression acts as an unfavorable survival marker, although some lineages such as SCLC show a favorable association.
HNSC, LIHC, and COAD are the cancer types where FRZB Mutation most reproducibly stratifies survival.