Across TCGA cell cohorts, RNA activity of the "Trans-synaptic signaling, modulating synaptic transmission" pathway is significantly associated with the shRNA dependency of multiple genes, with the LUNG_NSCLC_LUSC cohort showing a particularly strong set of associations.
The most reproducible pathway-associated genes across cancer lineages are FYCO1, PLCH2, and COASY, each associated with the pathway in up to 4 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 box plot shows the strongest association, FYCO1 grouped by "Trans-synaptic signaling, modulating synaptic transmission"-low versus -high activity in LUNG_NSCLC_LUSC.