Across TCGA pan-cancer cohorts, RERGL Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated RERGL data layer compared with 26 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher RERGL Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated RERGL expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
CESC, SCLC, and THCA are the cancer types where RERGL Mutation most reproducibly stratifies survival.