Across TCGA pan-cancer cohorts, NOMO2 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated NOMO2 data layer compared with 23 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in breast invasive carcinoma (BRCA), where higher NOMO2 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated NOMO2 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
BRCA, BLCA, and CESC are the cancer types where NOMO2 Mutation most reproducibly stratifies survival.