Across TCGA pan-cancer cohorts, STK38L Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated STK38L data layer compared with 23 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in uterine corpus endometrial carcinoma (UCEC), where higher STK38L Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated STK38L expression acts as an unfavorable survival marker.
UCEC, PRAD, and LUAD are the cancer types where STK38L Mutation most reproducibly stratifies survival.