Across TCGA pan-cancer cohorts, PHYHIP Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated PHYHIP data layer compared with 22 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in mesothelioma (MESO), where higher PHYHIP Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated PHYHIP expression acts as an unfavorable survival marker.
MESO and SARC are the cancer types where PHYHIP Mutation most reproducibly stratifies survival.