SLC1A2

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

Across TCGA patient cohorts, SLC1A2 mutation is significantly associated with the RNA expression of many other genes, with 4,688 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC1A2-associated genes across cancer lineages are C8orf89, TMEM138, and FAM177A1. Each is linked with SLC1A2 in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC1A2-to-partner and partner-to-SLC1A2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, C8orf89 grouped by SLC1A2-low versus SLC1A2-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC1A2→partner) and Y-score (partner→SLC1A2) 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
UCECC8orf89 →-0.231-2.149.006.00132
UCECTMEM138 →+0.261+2.425<.001<.00132
UCECFAM177A1 →+0.299+2.254.001.00532
UCECPI4K2A →+0.358+4.343<.001<.00132
UCECART3 →-0.332-1.485.009.00332
SKCMANKRD9 →+0.722+3.341.002.00532
Each partner links to its Q-omics profile. Showing the 6 strongest of 4,688 associations by consensus.

C8orf89 by SLC1A2 expression — UCEC

Box plot of C8orf89 in SLC1A2-low vs SLC1A2-high samples in UCEC.

Explore this box plot interactively →

Exploration