Across TCGA pan-cancer cohorts, DMBT1L1 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated DMBT1L1 data layer compared with 16 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher DMBT1L1 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated DMBT1L1 expression acts as an unfavorable survival marker.
CESC, THYM, and SARC are the cancer types where DMBT1L1 Mutation most reproducibly stratifies survival.