SLC66A1L

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

Across TCGA patient cohorts, SLC66A1L mutation is significantly associated with the RNA expression of many other genes, with 857 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SLC66A1L-associated genes across cancer lineages are USP9YP15, LIN7C, and IMMP1L. Each is linked with SLC66A1L in more than 1 cancer types. Because this analysis shows association rather than direction, both SLC66A1L-to-partner and partner-to-SLC66A1L results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, USP9YP15 grouped by SLC66A1L-low versus SLC66A1L-high in BRCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SLC66A1L→partner) and Y-score (partner→SLC66A1L) 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
BRCAUSP9YP15 →+0.084+8.471<.001.00531
UCECLIN7C →+0.586+2.815.003.00131
UCECIMMP1L →+0.446+2.332.002.00331
UCECMTA2 →+0.395+3.502.005.00231
UCECTMEM138 →+0.261+2.332.008.00331
UCECCPSF7 →+0.367+3.600.007.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 857 associations by consensus.

USP9YP15 by SLC66A1L expression — BRCA

Box plot of USP9YP15 in SLC66A1L-low vs SLC66A1L-high samples in BRCA.

Explore this box plot interactively →

Exploration