Across TCGA pan-cancer cohorts, IFT22 Mutation is linked to patient survival in 1 of 34 cancer types, making it a survival-associated IFT22 data layer compared with 24 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in lymphoid neoplasm diffuse large b-cell lymphoma (DLBC), where higher IFT22 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated IFT22 expression acts as an unfavorable survival marker.
DLBC are the cancer types where IFT22 Mutation most reproducibly stratifies survival.