Across TCGA pan-cancer cohorts, MIR503HG Mutation is linked to patient survival in 1 of 34 cancer types, making it a survival-associated MIR503HG data layer compared with 24 for mass-spec protein.
The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher MIR503HG Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated MIR503HG expression acts as an unfavorable survival marker.
OV are the cancer types where MIR503HG Mutation most reproducibly stratifies survival.