SLC16A8

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

Across TCGA cell cohorts, SLC16A8 mutation is significantly associated with the RNA expression of many other genes, with 4 significant associations in total. BLOOD_Leukemia shows the largest number of these associations.

The most reproducible SLC16A8-associated genes across cancer lineages are OR4M2, SPHKAP, and CST5. Each is linked with SLC16A8 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC16A8-to-partner and partner-to-SLC16A8 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, OR4M2 grouped by SLC16A8-low versus SLC16A8-high in SKIN.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC16A8→partner) and Y-score (partner→SLC16A8) 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
SKINOR4M2 →+0.156+4.977<.001.00731
LARGE_INTESTINESPHKAP →+0.006+5.415.007.00431
BLOOD_LeukemiaCST5 →+0.490+4.551<.001.00431
BLOOD_LeukemiaGDF5-AS1 →+0.029+4.481<.001.00411
Each partner links to its Q-omics profile. Showing the 4 strongest of 4 associations by consensus.

OR4M2 by SLC16A8 expression — SKIN

Box plot of OR4M2 in SLC16A8-low vs SLC16A8-high samples in SKIN.

Explore this box plot interactively →

Exploration