ARHGEF26

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

Across TCGA cell cohorts, ARHGEF26 mutation is significantly associated with the RNA expression of many other genes, with 487 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible ARHGEF26-associated genes across cancer lineages are NXF5, SLC30A7, and TDRD5. Each is linked with ARHGEF26 in more than 2 cancer types. Because this analysis shows association rather than direction, both ARHGEF26-to-partner and partner-to-ARHGEF26 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, NXF5 grouped by ARHGEF26-low versus ARHGEF26-high in CNS.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (ARHGEF26→partner) and Y-score (partner→ARHGEF26) 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
CNSNXF5 →+0.032+4.087<.001.00433
LARGE_INTESTINESLC30A7 →+0.515+2.936<.001<.00132
LARGE_INTESTINETDRD5 →+0.600+2.541<.001.00432
BLOOD_MyelomaOR2T35 →+0.086+4.807<.001.00631
BLOOD_MyelomaMUC5AC →+0.018+4.807<.001.00631
LIVERCLDN17 →+0.021+3.977<.001.00631
Each partner links to its Q-omics profile. Showing the 6 strongest of 487 associations by consensus.

NXF5 by ARHGEF26 expression — CNS

Box plot of NXF5 in ARHGEF26-low vs ARHGEF26-high samples in CNS.

Explore this box plot interactively →

Exploration