Across TCGA pan-cancer cohorts, SLC46A3 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated SLC46A3 data layer compared with 23 for mass-spec protein and 2 for mass-spec protein.
The strongest signal is observed in prostate adenocarcinoma (PRAD), where higher SLC46A3 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SLC46A3 expression acts as an unfavorable survival marker, although some lineages such as SKCM show a favorable association.
PRAD and SKCM are the cancer types where SLC46A3 Mutation most reproducibly stratifies survival.