Across TCGA pan-cancer cohorts, PRAMEF5 Mutation is linked to patient survival in 1 of 34 cancer types, making it a survival-associated PRAMEF5 data layer compared with 10 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher PRAMEF5 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated PRAMEF5 expression acts as an unfavorable survival marker.
CESC are the cancer types where PRAMEF5 Mutation most reproducibly stratifies survival.