Across TCGA pan-cancer cohorts, UBXN2B Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated UBXN2B data layer compared with 23 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher UBXN2B Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated UBXN2B expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
OV, UCEC, and LUSC are the cancer types where UBXN2B Mutation most reproducibly stratifies survival.