VIP

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

Across TCGA patient cohorts, VIP mutation is significantly associated with the total protein of many other genes, with 12 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible VIP-associated genes across cancer lineages are INPP4B, MEK1, and p27_pT198. Each is linked with VIP in more than 1 cancer types. Because this analysis shows association rather than direction, both VIP-to-partner and partner-to-VIP results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, INPP4B grouped by VIP-low versus VIP-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (VIP→partner) and Y-score (partner→VIP) 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
UCECINPP4B →-0.380-3.321.019.01031
UCECMEK1 →+0.590+3.459.001.00531
UCECp27_pT198 →+0.105+3.000.049.03631
UCECp38-MAPK →-0.166-2.979.044.03631
UCECTFRC →+0.689+2.321.009.03531
UCECTuberin →+0.382+2.321.004.03531
Each partner links to its Q-omics profile. Showing the 6 strongest of 12 associations by consensus.

INPP4B by VIP expression — UCEC

Box plot of INPP4B in VIP-low vs VIP-high samples in UCEC.

Explore this box plot interactively →

Exploration