Across TCGA pan-cancer cohorts, C6orf136 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated C6orf136 data layer compared with 25 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher C6orf136 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated C6orf136 expression acts as an unfavorable survival marker.
OV, LUSC, and SCLC are the cancer types where C6orf136 Mutation most reproducibly stratifies survival.