Across TCGA pan-cancer cohorts, BLOC1S3 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated BLOC1S3 data layer compared with 23 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in liver hepatocellular carcinoma (LIHC), where higher BLOC1S3 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated BLOC1S3 expression acts as an unfavorable survival marker.
LIHC and CHOL are the cancer types where BLOC1S3 Mutation most reproducibly stratifies survival.