SELENOM

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

Across TCGA patient cohorts, SELENOM mutation is significantly associated with the RNA expression of many other genes, with 24 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SELENOM-associated genes across cancer lineages are HSPE1-MOB4, MIR7702, and OR9Q2. Each is linked with SELENOM in more than 1 cancer types. Because this analysis shows association rather than direction, both SELENOM-to-partner and partner-to-SELENOM 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 (SELENOM→partner) and Y-score (partner→SELENOM) 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
UCECHSPE1-MOB4 →+0.228+3.432.003.00931
UCECMIR7702 →+0.537+5.738<.001<.00131
COADOR9Q2 →+0.070+6.721<.001<.00131
COADRNA5SP167 →+0.572+6.392.002.00131
COADMIR147A →+0.699+5.893<.001.00231
COADRNU7-11P →+0.842+5.145.002.00731
Each partner links to its Q-omics profile. Showing the 6 strongest of 24 associations by consensus.

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