SLC22A2

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

Across TCGA cell cohorts, SLC22A2 mutation is significantly associated with the RNA expression of many other genes, with 224 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible SLC22A2-associated genes across cancer lineages are MAGEB18, OR13C2, and PHF7. Each is linked with SLC22A2 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC22A2-to-partner and partner-to-SLC22A2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MAGEB18 grouped by SLC22A2-low versus SLC22A2-high in BLOOD_Leukemia.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC22A2→partner) and Y-score (partner→SLC22A2) 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_LeukemiaMAGEB18 →+0.096+4.567<.001.00132
SKINOR13C2 →+0.022+4.437<.001.00431
LARGE_INTESTINEPHF7 →+0.883+3.299<.001.00431
LARGE_INTESTINECRACD →+1.000+3.212.005.00631
LARGE_INTESTINESYF2 →+0.570+3.212<.001.00631
LARGE_INTESTINECCND2 →+2.507+3.212.001.00631
Each partner links to its Q-omics profile. Showing the 6 strongest of 224 associations by consensus.

MAGEB18 by SLC22A2 expression — BLOOD_Leukemia

Box plot of MAGEB18 in SLC22A2-low vs SLC22A2-high samples in BLOOD_Leukemia.

Explore this box plot interactively →

Exploration