VIM

mutation — cross-omics
Cross-omicsMUTATION → PROTEIN-RPPAPatientPairwise association · TCGA cohorts

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.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (VIM→partner) and Y-score (partner→VIM) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.
LineagePartner geneX-scoreY-scorep(X)p(Y)Sampling consensusLineage consensus
UCECNotch1 →+0.158+2.335.006.01832
UCECp62 Lck ligand →+0.546+3.710<.001<.00132
UCECFOXO3a_pS318_S321 →-0.113-1.990.027.03031
UCECINPP4B →-0.275-3.169.039.01831
UCECMAPK_pT202_Y204 →-0.478-1.807.013.02731
UCECNF-kB-p65_pS536 →-0.416-2.312.026.03431
Each partner links to its Q-omics profile. Showing the 6 strongest of 20 associations by consensus.

Notch1 by VIM expression — UCEC

Box plot of Notch1 in VIM-low vs VIM-high samples in UCEC.

Explore this box plot interactively →

Exploration