RNLS

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

Across TCGA patient cohorts, RNLS mutation is significantly associated with the RNA expression of many other genes, with 2,651 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RNLS-associated genes across cancer lineages are MTND4P33, MIR181A1, and RPS10P21. Each is linked with RNLS in more than 1 cancer types. Because this analysis shows association rather than direction, both RNLS-to-partner and partner-to-RNLS results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RNLS→partner) and Y-score (partner→RNLS) 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
SKCMMTND4P33 →+0.028+4.408<.001.00532
LUADMIR181A1 →+0.545+5.343.001.00632
HNSCRPS10P21 →+0.194+4.780<.001.00332
HNSCH2BP8 →+0.105+4.578<.001.00832
HNSCRNU7-10P →+0.913+5.266<.001.00132
UCECNPAS2 →-0.841-2.652<.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,651 associations by consensus.

Exploration