Across TCGA pan-cancer cohorts, RP2 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated RP2 data layer compared with 26 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher RP2 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated RP2 expression acts as an unfavorable survival marker.
CESC and SCLC are the cancer types where RP2 Mutation most reproducibly stratifies survival.