RETNLB

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

Across TCGA patient cohorts, RETNLB mutation is significantly associated with the RNA expression of many other genes, with 598 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RETNLB-associated genes across cancer lineages are MIR4529, RNA5SP412, and PSAT1P4. Each is linked with RETNLB in more than 2 cancer types. Because this analysis shows association rather than direction, both RETNLB-to-partner and partner-to-RETNLB results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MIR4529 grouped by RETNLB-low versus RETNLB-high in LUSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RETNLB→partner) and Y-score (partner→RETNLB) 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
LUSCMIR4529 →+0.284+3.370.004.00833
UCECRNA5SP412 →+0.578+2.481.002.00632
LUSCPSAT1P4 →+0.165+3.171<.001.00632
LUSCGAPDHP19 →+0.228+3.760<.001.00132
COADRN7SL575P →+0.466+5.017.009.00932
UCECMRPS11 →+0.501+3.212.001.00932
Each partner links to its Q-omics profile. Showing the 6 strongest of 598 associations by consensus.

MIR4529 by RETNLB expression — LUSC

Box plot of MIR4529 in RETNLB-low vs RETNLB-high samples in LUSC.

Explore this box plot interactively →

Exploration