OR1S2

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

Across TCGA patient cohorts, OR1S2 mutation is significantly associated with the RNA expression of many other genes, with 1,266 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible OR1S2-associated genes across cancer lineages are RN7SKP113, RN7SL840P, and RPSAP35. Each is linked with OR1S2 in more than 2 cancer types. Because this analysis shows association rather than direction, both OR1S2-to-partner and partner-to-OR1S2 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 (OR1S2→partner) and Y-score (partner→OR1S2) 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
SARCRN7SKP113 →+0.205+6.380<.001.00133
LUADRN7SL840P →+0.404+3.105<.001.00533
HNSCRPSAP35 →+0.061+5.888<.001<.00133
SKCMLYSMD4 →+0.437+2.632.001.00533
SCLCC12orf40 →+0.266+4.169<.001.00832
UCECNUDT4P2 →+0.053+2.899<.001.00332
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,266 associations by consensus.

Exploration