TSC22D1

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

Across TCGA patient cohorts, TSC22D1 mutation is significantly associated with the RNA expression of many other genes, with 2,221 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible TSC22D1-associated genes across cancer lineages are FOXO1B, RNU6-718P, and UHRF1. Each is linked with TSC22D1 in more than 2 cancer types. Because this analysis shows association rather than direction, both TSC22D1-to-partner and partner-to-TSC22D1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, FOXO1B grouped by TSC22D1-low versus TSC22D1-high in READ.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (TSC22D1→partner) and Y-score (partner→TSC22D1) 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
READFOXO1B →+0.146+5.039<.001.00833
CESCRNU6-718P →+0.251+6.584<.001<.00132
UCECUHRF1 →+0.766+1.903<.001<.00132
STADMIR5584 →+0.765+4.326.001.00732
READRN7SL578P →+0.172+5.039<.001.00832
LUSCSLC16A14P1 →+0.278+3.750<.001.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,221 associations by consensus.

FOXO1B by TSC22D1 expression — READ

Box plot of FOXO1B in TSC22D1-low vs TSC22D1-high samples in READ.

Explore this box plot interactively →

Exploration