BRD1

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

Across TCGA patient cohorts, BRD1 mutation is significantly associated with the RNA expression of many other genes, with 3,811 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible BRD1-associated genes across cancer lineages are SNRNP25, LRR1, and FH. Each is linked with BRD1 in more than 3 cancer types. Because this analysis shows association rather than direction, both BRD1-to-partner and partner-to-BRD1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SNRNP25 grouped by BRD1-low versus BRD1-high in COAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (BRD1→partner) and Y-score (partner→BRD1) 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
COADSNRNP25 →+0.472+3.847.004<.00134
COADLRR1 →+0.479+3.469.007.00234
UCECFH →+0.279+1.415.007.00234
COADPPP1R8 →+0.321+2.700.003.00634
UCECCHEK1 →+0.405+1.869.004.00424
UCECBUB3 →+0.392+2.397<.001<.00133
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,811 associations by consensus.

SNRNP25 by BRD1 expression — COAD

Box plot of SNRNP25 in BRD1-low vs BRD1-high samples in COAD.

Explore this box plot interactively →

Exploration