Across TCGA pan-cancer cohorts, B3GAT2 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated B3GAT2 data layer compared with 23 for mass-spec protein.
The strongest signal is observed in kidney renal clear cell carcinoma (KIRC), where higher B3GAT2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated B3GAT2 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
KIRC, ESCA, and BLCA are the cancer types where B3GAT2 Mutation most reproducibly stratifies survival.