Across TCGA pan-cancer cohorts, KIAA2013 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated KIAA2013 data layer compared with 25 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher KIAA2013 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated KIAA2013 expression acts as an unfavorable survival marker.
OV, LIHC, and ESCA are the cancer types where KIAA2013 Mutation most reproducibly stratifies survival.