Across TCGA patient cohorts, RNA activity of the Nuclear-transcribed mRNA poly(A) tail shortening pathway is significantly associated with the RNA expression of multiple genes, with the OV cohort showing a particularly strong set of associations.
The most reproducible pathway-associated genes across cancer lineages are C6orf141, BNIP1, and ACOT9, each associated with the pathway in up to 5 cancer types. Since the analysis shows associations rather than directional relationships, both pathway-to-partner and partner-to-pathway views are reported.
Each partner is linked to its corresponding Q-omics profile. The scatter plot shows the strongest association, Nuclear-transcribed mRNA poly(A) tail shortening activity versus C6orf141 in OV (Pearson r = 0.34).