RTKN2

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

Across TCGA patient cohorts, RTKN2 mutation is significantly associated with the RNA expression of many other genes, with 1,738 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RTKN2-associated genes across cancer lineages are MIR4659A, RNA5SP415, and GAGE2E. Each is linked with RTKN2 in more than 2 cancer types. Because this analysis shows association rather than direction, both RTKN2-to-partner and partner-to-RTKN2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MIR4659A grouped by RTKN2-low versus RTKN2-high in GBM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RTKN2→partner) and Y-score (partner→RTKN2) 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
GBMMIR4659A →+0.986+4.203<.001.00833
UCECRNA5SP415 →+0.442+1.974<.001.00333
GBMGAGE2E →+0.332+4.584<.001.00732
UCECRNVU1-28 →+0.545+1.742<.001.00132
READOR6K5P →+0.042+5.257<.001.00232
LUSCANKRD33B-AS1 →+0.416+4.287<.001.00832
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,738 associations by consensus.

MIR4659A by RTKN2 expression — GBM

Box plot of MIR4659A in RTKN2-low vs RTKN2-high samples in GBM.

Explore this box plot interactively →

Exploration