BRD9

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

Across TCGA patient cohorts, BRD9 mutation is significantly associated with the RNA expression of many other genes, with 3,754 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible BRD9-associated genes across cancer lineages are RNU6-391P, RPS15AP3, and MIR4488. Each is linked with BRD9 in more than 2 cancer types. Because this analysis shows association rather than direction, both BRD9-to-partner and partner-to-BRD9 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU6-391P grouped by BRD9-low versus BRD9-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (BRD9→partner) and Y-score (partner→BRD9) 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
SKCMRNU6-391P →+0.097+3.900<.001.00833
BLCARPS15AP3 →+0.118+5.788<.001.00333
LUSCMIR4488 →+0.671+5.093<.001.00833
OVARL2BPP5 →+0.097+3.945<.001.00532
UCECHDGFL2 →+0.476+2.263<.001<.00132
SKCMCTDSPL2P2 →+0.048+4.225<.001.00532
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,754 associations by consensus.

RNU6-391P by BRD9 expression — SKCM

Box plot of RNU6-391P in BRD9-low vs BRD9-high samples in SKCM.

Explore this box plot interactively →

Exploration