CNOT1

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

Across TCGA patient cohorts, CNOT1 mutation is significantly associated with the RNA expression of many other genes, with 6,228 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible CNOT1-associated genes across cancer lineages are PAPLN, ERCC2, and DCPS. Each is linked with CNOT1 in more than 5 cancer types. Because this analysis shows association rather than direction, both CNOT1-to-partner and partner-to-CNOT1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, PAPLN grouped by CNOT1-low versus CNOT1-high in BRCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (CNOT1→partner) and Y-score (partner→CNOT1) 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
BRCAPAPLN →-0.874-3.689<.001.00136
LUSCERCC2 →+0.446+3.348.003.00535
COADDCPS →+0.438+3.860<.001<.00135
COADCLUH →+0.455+2.097.001<.00135
STADMTMR4 →+0.490+2.338.003.00335
STADDDX19A →+0.368+3.000.001<.00135
Each partner links to its Q-omics profile. Showing the 6 strongest of 6,228 associations by consensus.

PAPLN by CNOT1 expression — BRCA

Box plot of PAPLN in CNOT1-low vs CNOT1-high samples in BRCA.

Explore this box plot interactively →

Exploration