NOP9

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

Across TCGA patient cohorts, NOP9 mutation is significantly associated with the RNA expression of many other genes, with 3,861 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NOP9-associated genes across cancer lineages are RNU1-17P, RNU6ATAC38P, and RNU6-1318P. Each is linked with NOP9 in more than 2 cancer types. Because this analysis shows association rather than direction, both NOP9-to-partner and partner-to-NOP9 results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NOP9→partner) and Y-score (partner→NOP9) 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
UCECRNU1-17P →+0.166+2.350.001.00233
LIHCRNU6ATAC38P →+0.368+6.008<.001.00232
BLCARNU6-1318P →+0.324+4.588<.001.00832
BLCARNU6-198P →+0.565+4.719<.001.00332
UCECSNORD82 →+0.389+1.717.002.00532
UCECNFYBP1 →+0.173+1.880<.001.00232
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,861 associations by consensus.

Exploration