Across TCGA patient cohorts, VIM mutation is significantly associated with the total protein of many other genes, with 20 significant associations in total. UCEC shows the largest number of these associations.
The most reproducible VIM-associated genes across cancer lineages are Notch1, p62 Lck ligand, and FOXO3a_pS318_S321. Each is linked with VIM in more than 1 cancer types. Because this analysis shows association rather than direction, both VIM-to-partner and partner-to-VIM results are reported.
Each partner links to its own Q-omics profile. The box plot shows the strongest example, Notch1 grouped by VIM-low versus VIM-high in UCEC.