NME9

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

Across TCGA patient cohorts, NME9 mutation is significantly associated with the RNA expression of many other genes, with 1,117 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NME9-associated genes across cancer lineages are MIR877, RNU6-1274P, and OR6K5P. Each is linked with NME9 in more than 2 cancer types. Because this analysis shows association rather than direction, both NME9-to-partner and partner-to-NME9 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MIR877 grouped by NME9-low versus NME9-high in HNSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NME9→partner) and Y-score (partner→NME9) 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
HNSCMIR877 →+0.337+5.241<.001.00733
READRNU6-1274P →+0.547+5.925<.001.00232
READOR6K5P →+0.057+6.257<.001.00132
BLCARNU7-56P →+0.528+5.147<.001.00332
SKCMRNU6-694P →+0.164+4.624<.001.00532
READPGBD4P2 →+0.162+6.257<.001.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,117 associations by consensus.

MIR877 by NME9 expression — HNSC

Box plot of MIR877 in NME9-low vs NME9-high samples in HNSC.

Explore this box plot interactively →

Exploration