Across TCGA pan-cancer cohorts, FAM169A Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated FAM169A data layer compared with 21 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher FAM169A Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated FAM169A expression acts as an unfavorable survival marker.
OV, LUSC, and COAD are the cancer types where FAM169A Mutation most reproducibly stratifies survival.