SLC22A1

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

Across TCGA cell cohorts, SLC22A1 mutation is significantly associated with the RNA expression of many other genes, with 24 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible SLC22A1-associated genes across cancer lineages are NLRP8, KLHL34, and PPIAL4F. Each is linked with SLC22A1 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC22A1-to-partner and partner-to-SLC22A1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, NLRP8 grouped by SLC22A1-low versus SLC22A1-high in OESOPHAGUS.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC22A1→partner) and Y-score (partner→SLC22A1) 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
OESOPHAGUSNLRP8 →+0.006+4.906<.001.00631
OESOPHAGUSKLHL34 →+0.013+4.906<.001.00631
OESOPHAGUSPPIAL4F →+0.060+4.906<.001.00631
BLOOD_LeukemiaCRYAA →+0.091+4.705<.001.00331
BLOOD_LeukemiaPRM3 →+0.067+5.569<.001.00131
BLOOD_LeukemiaDEFB125 →+0.036+5.060<.001.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 24 associations by consensus.

NLRP8 by SLC22A1 expression — OESOPHAGUS

Box plot of NLRP8 in SLC22A1-low vs SLC22A1-high samples in OESOPHAGUS.

Explore this box plot interactively →

Exploration