Across TCGA pan-cancer cohorts, MINDY4 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated MINDY4 data layer compared with 23 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in sarcoma (SARC), where higher MINDY4 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated MINDY4 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
SARC, ESCA, and UCEC are the cancer types where MINDY4 Mutation most reproducibly stratifies survival.