PEX11B

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

Across TCGA patient cohorts, PEX11B mutation is significantly associated with the RNA expression of many other genes, with 2,212 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PEX11B-associated genes across cancer lineages are RN7SL787P, LCN9, and RNA5SP137. Each is linked with PEX11B in more than 1 cancer types. Because this analysis shows association rather than direction, both PEX11B-to-partner and partner-to-PEX11B results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SL787P grouped by PEX11B-low versus PEX11B-high in BRCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PEX11B→partner) and Y-score (partner→PEX11B) 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
BRCARN7SL787P →+0.254+5.148<.001.00831
SKCMLCN9 →+0.131+5.080<.001.00431
BRCARNA5SP137 →+0.253+5.045.003.00931
BRCASNORD115-9 →+0.225+8.057<.001.00531
BRCAMIR595 →+0.346+5.610.004.00431
BRCATRGJ2 →+1.124+6.442<.001.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,212 associations by consensus.

RN7SL787P by PEX11B expression — BRCA

Box plot of RN7SL787P in PEX11B-low vs PEX11B-high samples in BRCA.

Explore this box plot interactively →

Exploration