BCHE

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

Across TCGA cell cohorts, BCHE mutation is significantly associated with the mutation status of many other genes, with 3,932 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible BCHE-associated genes across cancer lineages are RBM47, FLNB, and WDR33. Each is linked with BCHE in more than 4 cancer types. Because this analysis shows association rather than direction, both BCHE-to-partner and partner-to-BCHE results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RBM47 grouped by BCHE-low versus BCHE-high in CNS.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (BCHE→partner) and Y-score (partner→BCHE) 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
CNSRBM47 →+5.044+5.614.003.00315
BLOOD_LeukemiaFLNB →+2.260+3.101.002.00215
BONEWDR33 →+5.000+4.437.007.00714
BONELRFN2 →+5.000+4.437.007.00714
BONEKIT →+5.000+4.437.007.00714
BONEATAD5 →+5.000+4.437.007.00714
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,932 associations by consensus.

RBM47 by BCHE expression — CNS

Box plot of RBM47 in BCHE-low vs BCHE-high samples in CNS.

Explore this box plot interactively →

Exploration