CHD1L

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

Across TCGA patient cohorts, CHD1L mutation is significantly associated with the RNA expression of many other genes, with 1,079 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible CHD1L-associated genes across cancer lineages are MIR548AW, RNU6-905P, and ZMAT1. Each is linked with CHD1L in more than 2 cancer types. Because this analysis shows association rather than direction, both CHD1L-to-partner and partner-to-CHD1L results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MIR548AW grouped by CHD1L-low versus CHD1L-high in BRCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (CHD1L→partner) and Y-score (partner→CHD1L) 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
BRCAMIR548AW →+0.200+4.201<.001.00733
SKCMRNU6-905P →+0.144+3.098.004.00833
UCECZMAT1 →-0.653-2.523.001<.00132
UCECLPL →-0.518-1.807.005.00432
UCECRIC8A →+0.302+2.032.007.00532
SKCMNCAPH2 →+0.530+3.208.007.00932
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,079 associations by consensus.

MIR548AW by CHD1L expression — BRCA

Box plot of MIR548AW in CHD1L-low vs CHD1L-high samples in BRCA.

Explore this box plot interactively →

Exploration