Across TCGA pan-cancer cohorts, HOXC6 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated HOXC6 data layer compared with 29 for mass-spec protein.
The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher HOXC6 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated HOXC6 expression acts as an unfavorable survival marker.
OV, UCEC, and LIHC are the cancer types where HOXC6 Mutation most reproducibly stratifies survival.