RGN

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

Across TCGA cell cohorts, RGN mutation is significantly associated with the RNA expression of many other genes, with 3 significant associations in total. SKIN shows the largest number of these associations.

The most reproducible RGN-associated genes across cancer lineages are BHLHE23, OR52E8, and PNLIPRP2. Each is linked with RGN in more than 1 cancer types. Because this analysis shows association rather than direction, both RGN-to-partner and partner-to-RGN results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, BHLHE23 grouped by RGN-low versus RGN-high in SKIN.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RGN→partner) and Y-score (partner→RGN) 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
SKINBHLHE23 →+0.049+6.022<.001.00131
SKINOR52E8 →+0.032+5.415<.001.00431
BLOOD_LeukemiaPNLIPRP2 →+0.678+5.539<.001.00331
Each partner links to its Q-omics profile. Showing the 3 strongest of 3 associations by consensus.

BHLHE23 by RGN expression — SKIN

Box plot of BHLHE23 in RGN-low vs RGN-high samples in SKIN.

Explore this box plot interactively →

Exploration