ARHGEF9

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

Across TCGA patient cohorts, ARHGEF9 mutation is significantly associated with the RNA expression of many other genes, with 5,413 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible ARHGEF9-associated genes across cancer lineages are MIR3912, RNA5SP364, and CBX3P8. Each is linked with ARHGEF9 in more than 2 cancer types. Because this analysis shows association rather than direction, both ARHGEF9-to-partner and partner-to-ARHGEF9 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MIR3912 grouped by ARHGEF9-low versus ARHGEF9-high in CESC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (ARHGEF9→partner) and Y-score (partner→ARHGEF9) 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
CESCMIR3912 →+0.229+2.826.001.00633
HNSCRNA5SP364 →+0.557+4.122.001.00432
HNSCCBX3P8 →+0.052+4.636<.001.00632
READMIRLET7F1 →+0.573+4.533<.001.00432
READNPLP1 →+0.229+4.421<.001.00932
READMIR3619 →+1.035+4.361<.001.00632
Each partner links to its Q-omics profile. Showing the 6 strongest of 5,413 associations by consensus.

MIR3912 by ARHGEF9 expression — CESC

Box plot of MIR3912 in ARHGEF9-low vs ARHGEF9-high samples in CESC.

Explore this box plot interactively →

Exploration