DSCR8

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

Across TCGA patient cohorts, DSCR8 mutation is significantly associated with the RNA expression of many other genes, with 52 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible DSCR8-associated genes across cancer lineages are NTAN1P1, AQP7P5, and RNASE11. Each is linked with DSCR8 in more than 1 cancer types. Because this analysis shows association rather than direction, both DSCR8-to-partner and partner-to-DSCR8 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 (DSCR8→partner) and Y-score (partner→DSCR8) 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
UCECNTAN1P1 →+0.192+5.937.005.00231
UCECAQP7P5 →+0.111+5.694<.001.00331
UCECRNASE11 →+0.044+6.722<.001<.00131
UCECNF1P5 →+0.229+5.694<.001.00331
UCECOR51G2 →+0.158+5.299<.001.00631
UCECLINC01892 →+0.210+5.484<.001.00531
Each partner links to its Q-omics profile. Showing the 6 strongest of 52 associations by consensus.

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