RHOXF2B

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

Across TCGA patient cohorts, RHOXF2B mutation is significantly associated with the RNA expression of many other genes, with 349 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RHOXF2B-associated genes across cancer lineages are CDH12P2, RNU1-64P, and RNA5SP407. Each is linked with RHOXF2B in more than 1 cancer types. Because this analysis shows association rather than direction, both RHOXF2B-to-partner and partner-to-RHOXF2B 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 (RHOXF2B→partner) and Y-score (partner→RHOXF2B) 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
UCECCDH12P2 →+0.053+5.308<.001.00132
HNSCRNU1-64P →+0.823+7.954<.001.00831
HNSCRNA5SP407 →+0.238+7.954<.001.00831
UCECCOPS8P1 →+0.171+3.427<.001<.00131
UCECRNA5SP411 →+1.468+2.656<.001.00331
UCECRNA5SP412 →+0.895+2.704<.001.00431
Each partner links to its Q-omics profile. Showing the 6 strongest of 349 associations by consensus.

Exploration