SLC22A12

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

Across TCGA patient cohorts, SLC22A12 mutation is significantly associated with the RNA expression of many other genes, with 1,496 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC22A12-associated genes across cancer lineages are FEN1, EIF2B4, and PIMREG. Each is linked with SLC22A12 in more than 2 cancer types. Because this analysis shows association rather than direction, both SLC22A12-to-partner and partner-to-SLC22A12 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 (SLC22A12→partner) and Y-score (partner→SLC22A12) 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
LUADFEN1 →+0.633+2.596.006.00633
LUADEIF2B4 →+0.452+3.330<.001.00533
LUADPIMREG →+1.169+3.333<.001.00533
UCECPSMC3IP →+0.700+2.724<.001.00333
LUADMDC1 →+0.722+3.339<.001.00533
UCECARRDC1-AS1 →+0.412+2.721.001.00333
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,496 associations by consensus.

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