NBN

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

Across TCGA patient cohorts, NBN mutation is significantly associated with the RNA expression of many other genes, with 3,708 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NBN-associated genes across cancer lineages are MIR4797, RPS29P32, and RNU6-492P. Each is linked with NBN in more than 2 cancer types. Because this analysis shows association rather than direction, both NBN-to-partner and partner-to-NBN results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MIR4797 grouped by NBN-low versus NBN-high in READ.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NBN→partner) and Y-score (partner→NBN) 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
READMIR4797 →+0.790+5.054<.001.00133
UCECRPS29P32 →+0.349+1.883<.001.00433
HNSCRNU6-492P →+0.478+7.954<.001.00832
READRNU6-855P →+0.498+4.925<.001.00432
READXGY1 →+0.202+5.681<.001.00132
READRNU6-781P →+0.628+4.925<.001.00432
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,708 associations by consensus.

MIR4797 by NBN expression — READ

Box plot of MIR4797 in NBN-low vs NBN-high samples in READ.

Explore this box plot interactively →

Exploration