Across TCGA pan-cancer cohorts, EEF1AKMT2 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated EEF1AKMT2 data layer compared with 24 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in prostate adenocarcinoma (PRAD), where higher EEF1AKMT2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated EEF1AKMT2 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
PRAD and UCEC are the cancer types where EEF1AKMT2 Mutation most reproducibly stratifies survival.