Across TCGA pan-cancer cohorts, PRR23C Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated PRR23C data layer compared with 21 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher PRR23C Mutation is associated with better disease-free survival. In most high-consensus cancer types, elevated PRR23C expression acts as an unfavorable survival marker, although some lineages such as UCEC and SCLC show a favorable association.
UCEC, DLBC, and HNSC are the cancer types where PRR23C Mutation most reproducibly stratifies survival.