TSC22D2

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

Across TCGA patient cohorts, TSC22D2 mutation is significantly associated with the RNA expression of many other genes, with 4,582 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible TSC22D2-associated genes across cancer lineages are MIR4798, RNU1-139P, and RNU6-987P. Each is linked with TSC22D2 in more than 2 cancer types. Because this analysis shows association rather than direction, both TSC22D2-to-partner and partner-to-TSC22D2 results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (TSC22D2→partner) and Y-score (partner→TSC22D2) 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
LUADMIR4798 →+0.534+4.712.003.00733
HNSCRNU1-139P →+0.239+7.954<.001.00832
BLCARNU6-987P →+0.418+4.914<.001<.00132
SKCMMIR4288 →+0.267+4.328<.001.00732
SKCMHMGN1P31 →+0.066+4.797<.001.00332
BRCAMIR2392 →+0.344+7.471<.001.00832
Each partner links to its Q-omics profile. Showing the 6 strongest of 4,582 associations by consensus.

Exploration