SATB1

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

Across TCGA patient cohorts, SATB1 mutation is significantly associated with the RNA expression of many other genes, with 4,847 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SATB1-associated genes across cancer lineages are RN7SL248P, OXSM, and BUB3. Each is linked with SATB1 in more than 2 cancer types. Because this analysis shows association rather than direction, both SATB1-to-partner and partner-to-SATB1 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 (SATB1→partner) and Y-score (partner→SATB1) 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
UCECRN7SL248P →+0.043+2.552<.001.00333
UCECOXSM →+0.332+2.392<.001<.00133
UCECBUB3 →+0.434+2.323<.001<.00133
UCECSUPV3L1 →+0.329+1.595<.001<.00133
UCECMYO19 →+0.513+2.524<.001<.00133
UCECMICU1 →+0.265+1.462.005.00233
Each partner links to its Q-omics profile. Showing the 6 strongest of 4,847 associations by consensus.

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