Across TCGA pan-cancer cohorts, UBXN4 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated UBXN4 data layer compared with 26 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in skin cutaneous melanoma (SKCM), where higher UBXN4 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated UBXN4 expression acts as an unfavorable survival marker, although some lineages such as BLCA show a favorable association.
SKCM, CHOL, and BLCA are the cancer types where UBXN4 Mutation most reproducibly stratifies survival.