FANCB

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

Across TCGA patient cohorts, FANCB mutation is significantly associated with the RNA expression of many other genes, with 3,401 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FANCB-associated genes across cancer lineages are RN7SKP169, MIR6766, and HIRA. Each is linked with FANCB in more than 2 cancer types. Because this analysis shows association rather than direction, both FANCB-to-partner and partner-to-FANCB results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SKP169 grouped by FANCB-low versus FANCB-high in COAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FANCB→partner) and Y-score (partner→FANCB) 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
COADRN7SKP169 →+0.139+4.392.003.00633
BRCAMIR6766 →+0.501+4.575<.001.00932
UCECHIRA →+0.478+1.653<.001<.00132
UCECSNU13 →+0.239+1.915.002<.00132
UCECTBL1X →+0.462+1.632.001<.00132
UCECPGK1 →+0.655+1.830<.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,401 associations by consensus.

RN7SKP169 by FANCB expression — COAD

Box plot of RN7SKP169 in FANCB-low vs FANCB-high samples in COAD.

Explore this box plot interactively →

Exploration