Across TCGA pan-cancer cohorts, PRPSAP2 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated PRPSAP2 data layer compared with 25 for mass-spec protein and 7 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher PRPSAP2 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated PRPSAP2 expression acts as an unfavorable survival marker, although some lineages such as UCEC and SKCM show a favorable association.
CESC, LGG, and PRAD are the cancer types where PRPSAP2 Mutation most reproducibly stratifies survival.