Across TCGA pan-cancer cohorts, BNIP3L Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated BNIP3L data layer compared with 20 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher BNIP3L Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated BNIP3L expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
UCEC, BLCA, and KICH are the cancer types where BNIP3L Mutation most reproducibly stratifies survival.