SLC1A5

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

Across TCGA patient cohorts, SLC1A5 mutation is significantly associated with the RNA expression of many other genes, with 651 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC1A5-associated genes across cancer lineages are CFTRP3, KATNAL2, and UPP1. Each is linked with SLC1A5 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC1A5-to-partner and partner-to-SLC1A5 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, CFTRP3 grouped by SLC1A5-low versus SLC1A5-high in HNSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC1A5→partner) and Y-score (partner→SLC1A5) 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
HNSCCFTRP3 →+0.185+4.912<.001.00532
UCECKATNAL2 →-0.728-2.684<.001.00632
UCECUPP1 →+0.828+3.169<.001<.00132
UCECHOXC-AS1 →+0.837+2.230.001.00232
UCECMNX1 →+0.865+2.513.001.00132
PRADRNU6-1144P →+0.383+7.939<.001.00831
Each partner links to its Q-omics profile. Showing the 6 strongest of 651 associations by consensus.

CFTRP3 by SLC1A5 expression — HNSC

Box plot of CFTRP3 in SLC1A5-low vs SLC1A5-high samples in HNSC.

Explore this box plot interactively →

Exploration