NSF

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

Across TCGA patient cohorts, NSF mutation is significantly associated with the RNA expression of many other genes, with 365 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NSF-associated genes across cancer lineages are RNY3P11, RNA5SP379, and RN7SL98P. Each is linked with NSF in more than 1 cancer types. Because this analysis shows association rather than direction, both NSF-to-partner and partner-to-NSF results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNY3P11 grouped by NSF-low versus NSF-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NSF→partner) and Y-score (partner→NSF) 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
UCECRNY3P11 →+0.184+2.577.006.00632
UCECRNA5SP379 →+0.495+1.899<.001.00432
COADRN7SL98P →+0.268+5.693.001.00332
CESCRPL12P23 →+0.164+3.816<.001.00732
CESCCICP13 →+0.035+3.890<.001.00731
CESCRPS26P30 →+0.158+5.397<.001<.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 365 associations by consensus.

RNY3P11 by NSF expression — UCEC

Box plot of RNY3P11 in NSF-low vs NSF-high samples in UCEC.

Explore this box plot interactively →

Exploration