BHLHE23

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

Across TCGA patient cohorts, BHLHE23 mutation is significantly associated with the RNA expression of many other genes, with 7 significant associations in total. COAD shows the largest number of these associations.

The most reproducible BHLHE23-associated genes across cancer lineages are SNORD113-4, RNU6-1054P, and LINC01826. Each is linked with BHLHE23 in more than 1 cancer types. Because this analysis shows association rather than direction, both BHLHE23-to-partner and partner-to-BHLHE23 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SNORD113-4 grouped by BHLHE23-low versus BHLHE23-high in COAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (BHLHE23→partner) and Y-score (partner→BHLHE23) 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
COADSNORD113-4 →+1.287+5.541<.001<.00131
COADRNU6-1054P →+0.859+3.993<.001.00531
COADLINC01826 →+0.099+5.136<.001.00231
COADVENTXP7 →+0.184+4.868<.001<.00131
COADMIR4314 →+0.354+5.332<.001.00231
COADUBE2Q2P6 →+0.124+4.428<.001.00231
Each partner links to its Q-omics profile. Showing the 6 strongest of 7 associations by consensus.

SNORD113-4 by BHLHE23 expression — COAD

Box plot of SNORD113-4 in BHLHE23-low vs BHLHE23-high samples in COAD.

Explore this box plot interactively →

Exploration