VIT

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

Across TCGA patient cohorts, VIT mutation is significantly associated with the total protein of many other genes, with 41 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible VIT-associated genes across cancer lineages are 14-3-3_beta, C-Raf, and Cyclin-B1. Each is linked with VIT in more than 2 cancer types. Because this analysis shows association rather than direction, both VIT-to-partner and partner-to-VIT results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (VIT→partner) and Y-score (partner→VIT) 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
STAD14-3-3_beta →-0.212-3.000.045.03633
UCECC-Raf →+0.132+1.584.002.00833
UCECCyclin-B1 →+0.437+1.906.010.01433
STADeIF4E →+0.224+3.000.016.03632
SKCMc-Kit →-0.597-3.321.016.00932
UCECINPP4B →-0.228-2.087.019.00432
Each partner links to its Q-omics profile. Showing the 6 strongest of 41 associations by consensus.

Exploration