NHP2

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

Across TCGA patient cohorts, NHP2 mutation is significantly associated with the RNA expression of many other genes, with 100 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NHP2-associated genes across cancer lineages are RNU6-391P, RNY1P7, and CPLX3. Each is linked with NHP2 in more than 1 cancer types. Because this analysis shows association rather than direction, both NHP2-to-partner and partner-to-NHP2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU6-391P grouped by NHP2-low versus NHP2-high in BRCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NHP2→partner) and Y-score (partner→NHP2) 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
BRCARNU6-391P →+0.331+7.731<.001.00932
BRCARNY1P7 →+0.318+8.055<.001.00731
BRCACPLX3 →+0.154+8.055<.001.00731
BRCALINC00353 →+0.059+8.055<.001.00731
UCECHYKK →+0.457+3.332.003.00531
UCECC3orf62 →+0.429+3.354.004.00531
Each partner links to its Q-omics profile. Showing the 6 strongest of 100 associations by consensus.

RNU6-391P by NHP2 expression — BRCA

Box plot of RNU6-391P in NHP2-low vs NHP2-high samples in BRCA.

Explore this box plot interactively →

Exploration