NSL1

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

Across TCGA patient cohorts, NSL1 mutation is significantly associated with the RNA expression of many other genes, with 377 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NSL1-associated genes across cancer lineages are RNU6-558P, BRK1P1, and RNU6-63P. Each is linked with NSL1 in more than 1 cancer types. Because this analysis shows association rather than direction, both NSL1-to-partner and partner-to-NSL1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU6-558P grouped by NSL1-low versus NSL1-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NSL1→partner) and Y-score (partner→NSL1) 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
SKCMRNU6-558P →+0.455+4.235<.001.00132
SKCMBRK1P1 →+0.171+3.490.002.00832
BRCARNU6-63P →+0.357+4.386<.001.00832
SKCMRNU6-782P →+0.216+4.199<.001.00932
SKCMHMGN2P26 →+0.089+4.993<.001.00232
BRCAIGHD5-12 →+1.120+3.782<.001.00732
Each partner links to its Q-omics profile. Showing the 6 strongest of 377 associations by consensus.

RNU6-558P by NSL1 expression — SKCM

Box plot of RNU6-558P in NSL1-low vs NSL1-high samples in SKCM.

Explore this box plot interactively →

Exploration