NARS2

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

Across TCGA patient cohorts, NARS2 mutation is significantly associated with the RNA expression of many other genes, with 645 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NARS2-associated genes across cancer lineages are MIR511, LINC01831, and RNU6-706P. Each is linked with NARS2 in more than 1 cancer types. Because this analysis shows association rather than direction, both NARS2-to-partner and partner-to-NARS2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MIR511 grouped by NARS2-low versus NARS2-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NARS2→partner) and Y-score (partner→NARS2) 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
SKCMMIR511 →+0.223+5.163<.001.00232
SKCMLINC01831 →+0.182+3.744<.001.00332
LUSCRNU6-706P →+0.273+4.297<.001.00932
LUADRNA5SP72 →+0.520+5.584<.001.00232
LUADOR8X1P →+0.116+5.087<.001.00432
BLCAHLA-N →+0.289+3.948.002.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 645 associations by consensus.

MIR511 by NARS2 expression — SKCM

Box plot of MIR511 in NARS2-low vs NARS2-high samples in SKCM.

Explore this box plot interactively →

Exploration