MED19

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

Across TCGA patient cohorts, MED19 mutation is significantly associated with the RNA expression of many other genes, with 53 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible MED19-associated genes across cancer lineages are E2F6P1, F8A2, and RNU6-371P. Each is linked with MED19 in more than 1 cancer types. Because this analysis shows association rather than direction, both MED19-to-partner and partner-to-MED19 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, E2F6P1 grouped by MED19-low versus MED19-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (MED19→partner) and Y-score (partner→MED19) 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
UCECE2F6P1 →+0.037+4.245<.001.00632
UCECF8A2 →+0.033+3.472<.001.00431
COADRNU6-371P →+0.596+7.741<.001.00931
COADMIR1263 →+1.494+7.741<.001.00931
COADMIR1283-1 →+0.726+7.741<.001.00931
COADMIR1179 →+1.171+7.741<.001.00931
Each partner links to its Q-omics profile. Showing the 6 strongest of 53 associations by consensus.

E2F6P1 by MED19 expression — UCEC

Box plot of E2F6P1 in MED19-low vs MED19-high samples in UCEC.

Explore this box plot interactively →

Exploration