SELENOP

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

Across TCGA cell cohorts, SELENOP mutation is significantly associated with the RNA expression of many other genes, with 5 significant associations in total. SKIN shows the largest number of these associations.

The most reproducible SELENOP-associated genes across cancer lineages are TNP1, OR4C12, and HMHB1. Each is linked with SELENOP in more than 1 cancer types. Because this analysis shows association rather than direction, both SELENOP-to-partner and partner-to-SELENOP results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, TNP1 grouped by SELENOP-low versus SELENOP-high in LARGE_INTESTINE.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SELENOP→partner) and Y-score (partner→SELENOP) 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
LARGE_INTESTINETNP1 →+0.172+5.415<.001.00431
LUNG_NSCLC_LUADOR4C12 →+0.013+4.078<.001.00931
SKINHMHB1 →+0.038+4.022<.001.00631
SKINCCR8 →+0.027+3.345<.001.00731
SKINKRTAP22-2 →+0.083+4.022<.001.00631
Each partner links to its Q-omics profile. Showing the 5 strongest of 5 associations by consensus.

TNP1 by SELENOP expression — LARGE_INTESTINE

Box plot of TNP1 in SELENOP-low vs SELENOP-high samples in LARGE_INTESTINE.

Explore this box plot interactively →

Exploration