DCLRE1A

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

Across TCGA patient cohorts, DCLRE1A mutation is significantly associated with the RNA expression of many other genes, with 3,168 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible DCLRE1A-associated genes across cancer lineages are DDIT3, IDI1, and MTND1P22. Each is linked with DCLRE1A in more than 2 cancer types. Because this analysis shows association rather than direction, both DCLRE1A-to-partner and partner-to-DCLRE1A 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 (DCLRE1A→partner) and Y-score (partner→DCLRE1A) 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
UCECDDIT3 →+0.532+2.436<.001.00133
UCECIDI1 →+0.453+1.958.004.00233
LIHCMTND1P22 →+0.169+5.186<.001.00732
HNSCMT-TN →+0.341+4.822<.001.00632
HNSCRNU1-101P →+0.226+5.763<.001.00132
UCECDOC2B →-0.818-1.999.001.00232
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,168 associations by consensus.

Exploration