SLC22A14

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

Across TCGA cell cohorts, SLC22A14 mutation is significantly associated with the mutation status of many other genes, with 5,943 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible SLC22A14-associated genes across cancer lineages are MLH3, PRRC2A, and KMT2A. Each is linked with SLC22A14 in more than 4 cancer types. Because this analysis shows association rather than direction, both SLC22A14-to-partner and partner-to-SLC22A14 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MLH3 grouped by SLC22A14-low versus SLC22A14-high in BLOOD_Leukemia.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC22A14→partner) and Y-score (partner→SLC22A14) 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
BLOOD_LeukemiaMLH3 →+2.870+3.347.009.00915
LARGE_INTESTINEPRRC2A →+1.999+2.584<.001<.00115
SKINKMT2A →+2.736+2.963.004.00415
BLOOD_LeukemiaADAMTS19 →+3.548+3.845.003.00314
BLOOD_LeukemiaCNTN5 →+2.870+3.347.009.00914
SKINSACS →+2.473+3.139.002.00214
Each partner links to its Q-omics profile. Showing the 6 strongest of 5,943 associations by consensus.

MLH3 by SLC22A14 expression — BLOOD_Leukemia

Box plot of MLH3 in SLC22A14-low vs SLC22A14-high samples in BLOOD_Leukemia.

Explore this box plot interactively →

Exploration