Across TCGA pan-cancer cohorts, MICU2 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated MICU2 data layer compared with 19 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in prostate adenocarcinoma (PRAD), where higher MICU2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated MICU2 expression acts as an unfavorable survival marker.
PRAD and LIHC are the cancer types where MICU2 Mutation most reproducibly stratifies survival.