Across TCGA pan-cancer cohorts, SLC7A10 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated SLC7A10 data layer compared with 24 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in prostate adenocarcinoma (PRAD), where higher SLC7A10 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SLC7A10 expression acts as an unfavorable survival marker, although some lineages such as BLCA show a favorable association.
PRAD, UCEC, and BLCA are the cancer types where SLC7A10 Mutation most reproducibly stratifies survival.