Across TCGA pan-cancer cohorts, FRMPD2B Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated FRMPD2B data layer compared with 19 for mass-spec protein.
The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher FRMPD2B Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated FRMPD2B expression acts as an unfavorable survival marker.
OV, STAD, and LIHC are the cancer types where FRMPD2B Mutation most reproducibly stratifies survival.