Across TCGA pan-cancer cohorts, DBF4B Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated DBF4B data layer compared with 29 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher DBF4B Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated DBF4B expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
UCEC, KIRP, and PRAD are the cancer types where DBF4B Mutation most reproducibly stratifies survival.