SLC22A10

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

Across TCGA patient cohorts, SLC22A10 mutation is significantly associated with the RNA expression of many other genes, with 1,947 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC22A10-associated genes across cancer lineages are FAM207CP, TEMN3-AS1, and MIR4733. Each is linked with SLC22A10 in more than 2 cancer types. Because this analysis shows association rather than direction, both SLC22A10-to-partner and partner-to-SLC22A10 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 (SLC22A10→partner) and Y-score (partner→SLC22A10) 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
COADFAM207CP →+0.097+5.412<.001.00133
LUSCTEMN3-AS1 →+0.208+3.337<.001.00633
LIHCMIR4733 →+0.426+6.169<.001<.00132
UCECALDOA →+0.415+2.643.004<.00132
SKCMFAM177A1 →+0.341+2.246.001.00132
UCECAP1S3 →+0.606+3.000<.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,947 associations by consensus.

Exploration