SLC22A4

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

Across TCGA patient cohorts, SLC22A4 mutation is significantly associated with the RNA expression of many other genes, with 1,935 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC22A4-associated genes across cancer lineages are RN7SL248P, RNA5SP282, and RNU6-964P. Each is linked with SLC22A4 in more than 3 cancer types. Because this analysis shows association rather than direction, both SLC22A4-to-partner and partner-to-SLC22A4 results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC22A4→partner) and Y-score (partner→SLC22A4) 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
UCECRN7SL248P →+0.051+2.915<.001.00734
SKCMRNA5SP282 →+0.535+5.075<.001.00132
SKCMRNU6-964P →+0.680+4.215<.001.00932
LUADELOA3P →+0.053+5.315<.001.00332
LUSCRNU6-1306P →+0.454+4.236.001.00832
COADRPL31P20 →+0.334+5.145.001.00732
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,935 associations by consensus.

Exploration