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.