Across TCGA pan-cancer cohorts, PGAP3 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated PGAP3 data layer compared with 24 for mass-spec protein and 2 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher PGAP3 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated PGAP3 expression acts as an unfavorable survival marker.
CESC and SKCM are the cancer types where PGAP3 Mutation most reproducibly stratifies survival.