NFE2L2

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

Across TCGA patient cohorts, NFE2L2 mutation is significantly associated with the RNA expression of many other genes, with 7,766 significant associations in total. LUSC shows the largest number of these associations.

The most reproducible NFE2L2-associated genes across cancer lineages are BLVRB, TNFSF9, and ALDH3A1. Each is linked with NFE2L2 in more than 6 cancer types. Because this analysis shows association rather than direction, both NFE2L2-to-partner and partner-to-NFE2L2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, BLVRB grouped by NFE2L2-low versus NFE2L2-high in BLCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NFE2L2→partner) and Y-score (partner→NFE2L2) 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
BLCABLVRB →+0.839+2.465<.001.00137
BLCATNFSF9 →+1.405+3.714<.001<.00137
BLCAALDH3A1 →+4.291+2.714<.001.00237
HNSCPANX2 →+2.310+4.011<.001<.00136
ESCACABYR →+2.965+3.486<.001.00127
LUSCSRXN1 →+2.107+3.510<.001<.00136
Each partner links to its Q-omics profile. Showing the 6 strongest of 7,766 associations by consensus.

BLVRB by NFE2L2 expression — BLCA

Box plot of BLVRB in NFE2L2-low vs NFE2L2-high samples in BLCA.

Explore this box plot interactively →

Exploration