RARG

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

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

The most reproducible RARG-associated genes across cancer lineages are NPY2R, IQCF6, and KCNU1. Each is linked with RARG in more than 1 cancer types. Because this analysis shows association rather than direction, both RARG-to-partner and partner-to-RARG results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, NPY2R grouped by RARG-low versus RARG-high in LARGE_INTESTINE.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RARG→partner) and Y-score (partner→RARG) 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_INTESTINENPY2R →+0.004+3.632<.001.00331
LARGE_INTESTINEIQCF6 →+0.228+3.882<.001.00131
LARGE_INTESTINEKCNU1 →+0.041+3.345.001.00731
LARGE_INTESTINEKRTAP7-1 →+0.040+4.022<.001.00631
BLOOD_LeukemiaASZ1 →+0.124+4.152<.001.00931
Each partner links to its Q-omics profile. Showing the 5 strongest of 5 associations by consensus.

NPY2R by RARG expression — LARGE_INTESTINE

Box plot of NPY2R in RARG-low vs RARG-high samples in LARGE_INTESTINE.

Explore this box plot interactively →

Exploration