BHLHE22

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

Across TCGA cell cohorts, BHLHE22 mutation is significantly associated with the RNA expression of many other genes, with 20 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible BHLHE22-associated genes across cancer lineages are FAM170B, CHCHD4, and RRH. Each is linked with BHLHE22 in more than 1 cancer types. Because this analysis shows association rather than direction, both BHLHE22-to-partner and partner-to-BHLHE22 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, FAM170B grouped by BHLHE22-low versus BHLHE22-high in CNS.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (BHLHE22→partner) and Y-score (partner→BHLHE22) 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
CNSFAM170B →+0.138+4.981<.001.00831
LARGE_INTESTINECHCHD4 →+0.564+3.067.006.00931
LARGE_INTESTINERRH →+0.232+3.295.001.00631
LARGE_INTESTINERPE →+0.435+3.160.003.00631
LARGE_INTESTINEZFP2 →+0.576+3.082<.001.00731
LARGE_INTESTINEDAZ4 →+0.109+2.977.008.00631
Each partner links to its Q-omics profile. Showing the 6 strongest of 20 associations by consensus.

FAM170B by BHLHE22 expression — CNS

Box plot of FAM170B in BHLHE22-low vs BHLHE22-high samples in CNS.

Explore this box plot interactively →

Exploration