Across TCGA pan-cancer cohorts, SH3D21 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated SH3D21 data layer compared with 24 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in breast invasive carcinoma (BRCA), where higher SH3D21 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SH3D21 expression acts as an unfavorable survival marker.
BRCA, BLCA, and UCEC are the cancer types where SH3D21 Mutation most reproducibly stratifies survival.