SLC12A2

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

Across TCGA cell cohorts, SLC12A2 mutation is significantly associated with the RNA expression of many other genes, with 235 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible SLC12A2-associated genes across cancer lineages are AVP, DENND3, and MAP3K8. Each is linked with SLC12A2 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC12A2-to-partner and partner-to-SLC12A2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, AVP grouped by SLC12A2-low versus SLC12A2-high in CNS.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC12A2→partner) and Y-score (partner→SLC12A2) 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
CNSAVP →+0.072+4.981<.001<.00132
LARGE_INTESTINEDENND3 →-0.890-3.243.004.00332
LARGE_INTESTINEMAP3K8 →-0.886-3.416.001.00232
LARGE_INTESTINETTC33 →+0.612+3.502.004.00132
LARGE_INTESTINEGSN →-1.731-3.416<.001.00232
LARGE_INTESTINEREG1B →+1.432+2.196.003.00432
Each partner links to its Q-omics profile. Showing the 6 strongest of 235 associations by consensus.

AVP by SLC12A2 expression — CNS

Box plot of AVP in SLC12A2-low vs SLC12A2-high samples in CNS.

Explore this box plot interactively →

Exploration