NR2F6

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

Across TCGA patient cohorts, NR2F6 mutation is significantly associated with the total protein of many other genes, with 3 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NR2F6-associated genes across cancer lineages are VHL, Ku80, and Smad1. Each is linked with NR2F6 in more than 1 cancer types. Because this analysis shows association rather than direction, both NR2F6-to-partner and partner-to-NR2F6 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, VHL grouped by NR2F6-low versus NR2F6-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NR2F6→partner) and Y-score (partner→NR2F6) 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
UCECVHL →-1.007-3.000.010.03731
UCECKu80 →+0.277+3.013.043.01911
UCECSmad1 →+0.186+3.000.040.03711
Each partner links to its Q-omics profile. Showing the 3 strongest of 3 associations by consensus.

VHL by NR2F6 expression — UCEC

Box plot of VHL in NR2F6-low vs NR2F6-high samples in UCEC.

Explore this box plot interactively →

Exploration