Across TCGA pan-cancer cohorts, RBPJL Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated RBPJL data layer compared with 22 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher RBPJL Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated RBPJL expression acts as an unfavorable survival marker.
OV, KIRC, and HNSC are the cancer types where RBPJL Mutation most reproducibly stratifies survival.