Across TCGA pan-cancer cohorts, POMZP3 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated POMZP3 data layer compared with 20 for mass-spec protein.
The strongest signal is observed in mesothelioma (MESO), where higher POMZP3 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated POMZP3 expression acts as an unfavorable survival marker.
MESO and UCEC are the cancer types where POMZP3 Mutation most reproducibly stratifies survival.