ARHGEF39

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

Across TCGA cell cohorts, ARHGEF39 mutation is significantly associated with the RNA expression of many other genes, with 3 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible ARHGEF39-associated genes across cancer lineages are FAM187B, UTF1, and ENTHD1. Each is linked with ARHGEF39 in more than 1 cancer types. Because this analysis shows association rather than direction, both ARHGEF39-to-partner and partner-to-ARHGEF39 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, FAM187B grouped by ARHGEF39-low versus ARHGEF39-high in BLOOD_Lymphoma.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (ARHGEF39→partner) and Y-score (partner→ARHGEF39) 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
BLOOD_LymphomaFAM187B →+0.052+5.643<.001.00231
LARGE_INTESTINEUTF1 →+0.018+3.632<.001.00331
LARGE_INTESTINEENTHD1 →+0.030+3.554.001.00731
Each partner links to its Q-omics profile. Showing the 3 strongest of 3 associations by consensus.

FAM187B by ARHGEF39 expression — BLOOD_Lymphoma

Box plot of FAM187B in ARHGEF39-low vs ARHGEF39-high samples in BLOOD_Lymphoma.

Explore this box plot interactively →

Exploration