SLC12A9

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

Across TCGA cell cohorts, SLC12A9 mutation is significantly associated with the RNA expression of many other genes, with 347 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible SLC12A9-associated genes across cancer lineages are HES3, DEFB133, and RBMY1A1. Each is linked with SLC12A9 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC12A9-to-partner and partner-to-SLC12A9 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, HES3 grouped by SLC12A9-low versus SLC12A9-high in CNS.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC12A9→partner) and Y-score (partner→SLC12A9) 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
CNSHES3 →+0.032+4.321<.001.00931
CNSDEFB133 →+0.035+5.357<.001.00131
OVARYRBMY1A1 →+0.143+5.807<.001.00131
LUNG_NSCLC_LUADZBTB16 →+0.395+3.482<.001.00831
LUNG_NSCLC_LUADPRMT8 →+0.422+3.602<.001.00631
LUNG_NSCLC_LUADASZ1 →+0.482+3.157<.001.00831
Each partner links to its Q-omics profile. Showing the 6 strongest of 347 associations by consensus.

HES3 by SLC12A9 expression — CNS

Box plot of HES3 in SLC12A9-low vs SLC12A9-high samples in CNS.

Explore this box plot interactively →

Exploration