NOL4L

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

Across TCGA patient cohorts, NOL4L mutation is significantly associated with the RNA expression of many other genes, with 1,931 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NOL4L-associated genes across cancer lineages are OR10H4, LINC01072, and NF1P4. Each is linked with NOL4L in more than 2 cancer types. Because this analysis shows association rather than direction, both NOL4L-to-partner and partner-to-NOL4L 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 (NOL4L→partner) and Y-score (partner→NOL4L) 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
CESCOR10H4 →+0.047+4.020<.001.00933
CESCLINC01072 →+0.121+3.345<.001.00832
CESCNF1P4 →+0.019+5.263<.001.00132
CESCRN7SL248P →+0.090+5.263<.001.00132
UCECPSAT1P4 →+0.107+1.563.002.00232
UCECC18orf25 →+0.378+2.818.002.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,931 associations by consensus.

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