SLC22A23

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

Across TCGA cell cohorts, SLC22A23 mutation is significantly associated with the drug of many other genes, with 37 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible SLC22A23-associated genes across cancer lineages are Alisertib, RO-3306, and Niraparib. Each is linked with SLC22A23 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC22A23-to-partner and partner-to-SLC22A23 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Alisertib grouped by SLC22A23-low versus SLC22A23-high in LARGE_INTESTINE.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC22A23→partner) and Y-score (partner→SLC22A23) 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_INTESTINEAlisertib →+0.924+3.061.004.01031
LARGE_INTESTINERO-3306 →+0.555+2.807.030.04631
LARGE_INTESTINENiraparib →+0.460+2.700.003.03031
LARGE_INTESTINE50869 →+0.405+3.064.034.00931
LARGE_INTESTINEBPD-00008900 →+0.435+2.655.030.04431
LARGE_INTESTINECP724714 →+0.338+2.874.034.02131
Each partner links to its Q-omics profile. Showing the 6 strongest of 37 associations by consensus.

Alisertib by SLC22A23 expression — LARGE_INTESTINE

Box plot of Alisertib in SLC22A23-low vs SLC22A23-high samples in LARGE_INTESTINE.

Explore this box plot interactively →

Exploration