Across TCGA pan-cancer cohorts, PROKR2 Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated PROKR2 data layer compared with 17 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher PROKR2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated PROKR2 expression acts as an unfavorable survival marker, although some lineages such as SKCM and LUSC show a favorable association.
OV, UCEC, and PRAD are the cancer types where PROKR2 Mutation most reproducibly stratifies survival.