Across TCGA pan-cancer cohorts, SIRPB1 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated SIRPB1 data layer compared with 22 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in rectum adenocarcinoma (READ), where higher SIRPB1 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SIRPB1 expression acts as an unfavorable survival marker, although some lineages such as SKCM show a favorable association.
READ, BLCA, and BRCA are the cancer types where SIRPB1 Mutation most reproducibly stratifies survival.