DCLRE1B

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

Across TCGA patient cohorts, DCLRE1B mutation is significantly associated with the RNA expression of many other genes, with 695 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible DCLRE1B-associated genes across cancer lineages are RNU6-275P, CDT1, and RN7SL248P. Each is linked with DCLRE1B in more than 2 cancer types. Because this analysis shows association rather than direction, both DCLRE1B-to-partner and partner-to-DCLRE1B results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU6-275P grouped by DCLRE1B-low versus DCLRE1B-high in LUAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (DCLRE1B→partner) and Y-score (partner→DCLRE1B) 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
LUADRNU6-275P →+0.519+5.157<.001.00733
UCECCDT1 →+0.665+2.202.002.00132
UCECRN7SL248P →+0.056+3.059<.001.00532
SKCMVAC14 →+0.454+3.407.007.00432
COADSRGAP3-AS1 →+0.223+4.790<.001.00632
BLCAMIR618 →+0.178+4.296<.001.00632
Each partner links to its Q-omics profile. Showing the 6 strongest of 695 associations by consensus.

RNU6-275P by DCLRE1B expression — LUAD

Box plot of RNU6-275P in DCLRE1B-low vs DCLRE1B-high samples in LUAD.

Explore this box plot interactively →

Exploration