BHLHE22

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

Across TCGA patient cohorts, BHLHE22 mutation is significantly associated with the RNA expression of many other genes, with 2,313 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible BHLHE22-associated genes across cancer lineages are TMEM252-DT, TRAJ12, and TRAJ11. 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, TMEM252-DT grouped by BHLHE22-low versus BHLHE22-high in HNSC.

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
HNSCTMEM252-DT →+0.037+4.536.001.00532
CESCTRAJ12 →+0.920+4.608<.001.00132
CESCTRAJ11 →+0.686+4.060<.001.00432
UCECSENP3-EIF4A1 →+0.079+1.523.005.00732
UCECHMGB1P24 →+0.233+3.906.001<.00132
UCECCCL3 →+0.835+1.671<.001.00732
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,313 associations by consensus.

TMEM252-DT by BHLHE22 expression — HNSC

Box plot of TMEM252-DT in BHLHE22-low vs BHLHE22-high samples in HNSC.

Explore this box plot interactively →

Exploration