Across TCGA pan-cancer cohorts, PPP1R3G Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated PPP1R3G data layer compared with 21 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher PPP1R3G Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated PPP1R3G expression acts as an unfavorable survival marker.
UCEC, MESO, and COAD are the cancer types where PPP1R3G Mutation most reproducibly stratifies survival.