SLC22A8

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

Across TCGA patient cohorts, SLC22A8 mutation is significantly associated with the RNA expression of many other genes, with 2,659 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC22A8-associated genes across cancer lineages are FAF1, CIDECP1, and E2F1. Each is linked with SLC22A8 in more than 2 cancer types. Because this analysis shows association rather than direction, both SLC22A8-to-partner and partner-to-SLC22A8 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, FAF1 grouped by SLC22A8-low versus SLC22A8-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC22A8→partner) and Y-score (partner→SLC22A8) 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
UCECFAF1 →+0.255+2.243.005.00533
UCECCIDECP1 →+0.340+2.748<.001<.00133
UCECE2F1 →+0.597+2.861.005.00133
UCECCHAF1A →+0.579+2.136<.001<.00133
UCECACBD5 →+0.437+1.836.003.00133
UCECUFM1 →+0.460+1.606.001.00333
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,659 associations by consensus.

FAF1 by SLC22A8 expression — UCEC

Box plot of FAF1 in SLC22A8-low vs SLC22A8-high samples in UCEC.

Explore this box plot interactively →

Exploration