Across TCGA pan-cancer cohorts, RHBDD3 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated RHBDD3 data layer compared with 25 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in skin cutaneous melanoma (SKCM), where higher RHBDD3 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated RHBDD3 expression acts as an unfavorable survival marker.
SKCM, READ, and CESC are the cancer types where RHBDD3 Mutation most reproducibly stratifies survival.