Across TCGA pan-cancer cohorts, DIO3 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated DIO3 data layer compared with 20 for mass-spec protein.
The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher DIO3 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated DIO3 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
OV, ESCA, and UCEC are the cancer types where DIO3 Mutation most reproducibly stratifies survival.