SLC18B1

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

Across TCGA cell cohorts, SLC18B1 mutation is significantly associated with the RNA expression of many other genes, with 10 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible SLC18B1-associated genes across cancer lineages are CDY2A, IFNA4, and FAM240A. Each is linked with SLC18B1 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC18B1-to-partner and partner-to-SLC18B1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, CDY2A grouped by SLC18B1-low versus SLC18B1-high in CNS.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC18B1→partner) and Y-score (partner→SLC18B1) 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
CNSCDY2A →+0.009+4.321<.001.00931
CNSIFNA4 →+0.160+4.321<.001.00931
CNSFAM240A →+0.012+4.169.004.00831
LARGE_INTESTINEPRSS54 →+0.038+3.345<.001.00731
LARGE_INTESTINECNMD →+0.030+3.453<.001.00931
LARGE_INTESTINEUTF1 →+0.018+3.632<.001.00331
Each partner links to its Q-omics profile. Showing the 6 strongest of 10 associations by consensus.

CDY2A by SLC18B1 expression — CNS

Box plot of CDY2A in SLC18B1-low vs SLC18B1-high samples in CNS.

Explore this box plot interactively →

Exploration