SLC14A1

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

Across TCGA cell cohorts, SLC14A1 mutation is significantly associated with the RNA expression of many other genes, with 7 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible SLC14A1-associated genes across cancer lineages are KIR2DL3, PRAMEF20, and TECRL. Each is linked with SLC14A1 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC14A1-to-partner and partner-to-SLC14A1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, KIR2DL3 grouped by SLC14A1-low versus SLC14A1-high in CNS.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC14A1→partner) and Y-score (partner→SLC14A1) 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
CNSKIR2DL3 →+0.025+4.981<.001.00831
LARGE_INTESTINEPRAMEF20 →+0.012+4.437<.001.00431
LARGE_INTESTINETECRL →+0.017+4.562<.001<.00131
LARGE_INTESTINEOR5V1 →+0.008+4.437<.001.00431
SKINC2CD4B →+0.041+4.684<.001.00231
BLOOD_LymphomaOR2AP1 →+0.025+4.867<.001.00931
Each partner links to its Q-omics profile. Showing the 6 strongest of 7 associations by consensus.

KIR2DL3 by SLC14A1 expression — CNS

Box plot of KIR2DL3 in SLC14A1-low vs SLC14A1-high samples in CNS.

Explore this box plot interactively →

Exploration