NARS1

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

Across TCGA patient cohorts, NARS1 mutation is significantly associated with the RNA expression of many other genes, with 3,397 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NARS1-associated genes across cancer lineages are RN7SL596P, CCNYL3, and PAXIP1. Each is linked with NARS1 in more than 1 cancer types. Because this analysis shows association rather than direction, both NARS1-to-partner and partner-to-NARS1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SL596P grouped by NARS1-low versus NARS1-high in BRCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NARS1→partner) and Y-score (partner→NARS1) 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
BRCARN7SL596P →+0.232+4.448<.001.00632
BRCACCNYL3 →+0.041+6.725<.001<.00132
UCECPAXIP1 →+0.412+2.201.001<.00132
UCECTMUB1 →+0.319+3.016.007<.00132
UCECNUDT2 →+0.483+2.201.001<.00132
UCECCIAO2B →+0.381+1.895.001.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,397 associations by consensus.

RN7SL596P by NARS1 expression — BRCA

Box plot of RN7SL596P in NARS1-low vs NARS1-high samples in BRCA.

Explore this box plot interactively →

Exploration