Across TCGA pan-cancer cohorts, PARG Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated PARG data layer compared with 22 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 PARG Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated PARG expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
CESC, BLCA, and SARC are the cancer types where PARG Mutation most reproducibly stratifies survival.