Across TCGA pan-cancer cohorts, SEL1L Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated SEL1L data layer compared with 21 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 SEL1L Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SEL1L expression acts as an unfavorable survival marker.
CESC, ACC, and SCLC are the cancer types where SEL1L Mutation most reproducibly stratifies survival.