Across TCGA pan-cancer cohorts, DMAC2L Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated DMAC2L data layer compared with 25 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher DMAC2L Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated DMAC2L expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
CESC, SKCM, and UCEC are the cancer types where DMAC2L Mutation most reproducibly stratifies survival.