Across TCGA pan-cancer cohorts, U2AF1L4 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated U2AF1L4 data layer compared with 28 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in skin cutaneous melanoma (SKCM), where higher U2AF1L4 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated U2AF1L4 expression acts as an unfavorable survival marker.
SKCM, READ, and LIHC are the cancer types where U2AF1L4 Mutation most reproducibly stratifies survival.