ADH1C

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

Across TCGA patient cohorts, ADH1C mutation is significantly associated with the total protein of many other genes, with 34 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible ADH1C-associated genes across cancer lineages are eIF4E, FoxM1, and Rb_pS807_S811. Each is linked with ADH1C in more than 1 cancer types. Because this analysis shows association rather than direction, both ADH1C-to-partner and partner-to-ADH1C results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, eIF4E grouped by ADH1C-low versus ADH1C-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (ADH1C→partner) and Y-score (partner→ADH1C) 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
UCECeIF4E →+0.165+2.820.037.03532
UCECFoxM1 →+0.222+2.662.022<.00132
SKCMRb_pS807_S811 →+0.400+2.115.003.01531
SKCMSrc →-0.239-2.058.001<.00131
SKCMTransglutaminase →-0.137-2.415.015.00331
SKCMCaveolin-1 →-0.475-1.765.016.01231
Each partner links to its Q-omics profile. Showing the 6 strongest of 34 associations by consensus.

eIF4E by ADH1C expression — UCEC

Box plot of eIF4E in ADH1C-low vs ADH1C-high samples in UCEC.

Explore this box plot interactively →

Exploration