NR2F2

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

Across TCGA patient cohorts, NR2F2 mutation is significantly associated with the RNA expression of many other genes, with 4,341 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NR2F2-associated genes across cancer lineages are RNA5SP528, USP9YP10, and RNA5SP149. Each is linked with NR2F2 in more than 1 cancer types. Because this analysis shows association rather than direction, both NR2F2-to-partner and partner-to-NR2F2 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 (NR2F2→partner) and Y-score (partner→NR2F2) 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
LIHCRNA5SP528 →+0.355+4.758<.001.00632
LGGUSP9YP10 →+0.049+7.977<.001.00732
HNSCRNA5SP149 →+0.376+4.578<.001.00832
LIHCOR8B10P →+0.038+4.544.004.00932
CESCMIR4690 →+0.865+4.101<.001.00432
UCECAURKB →+0.693+3.016<.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 4,341 associations by consensus.

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