DCLRE1C

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

Across TCGA patient cohorts, DCLRE1C mutation is significantly associated with the RNA expression of many other genes, with 3,207 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible DCLRE1C-associated genes across cancer lineages are CCDC11P1, OR5G5P, and RNU6-937P. Each is linked with DCLRE1C in more than 2 cancer types. Because this analysis shows association rather than direction, both DCLRE1C-to-partner and partner-to-DCLRE1C results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, CCDC11P1 grouped by DCLRE1C-low versus DCLRE1C-high in HNSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (DCLRE1C→partner) and Y-score (partner→DCLRE1C) 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
HNSCCCDC11P1 →+0.024+5.351<.001.00233
HNSCOR5G5P →+0.051+3.748<.001.00833
UCECRNU6-937P →+0.294+1.663.004.00233
CESCMTND5P13 →+0.035+4.103<.001.00232
CESCRNU7-35P →+0.283+5.584<.001.00132
HNSCLINC01674 →+0.053+4.754.002.00532
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,207 associations by consensus.

CCDC11P1 by DCLRE1C expression — HNSC

Box plot of CCDC11P1 in DCLRE1C-low vs DCLRE1C-high samples in HNSC.

Explore this box plot interactively →

Exploration