NPAS2

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

Across TCGA patient cohorts, NPAS2 mutation is significantly associated with the total protein of many other genes, with 40 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NPAS2-associated genes across cancer lineages are PCNA, eIF4G, and FoxM1. Each is linked with NPAS2 in more than 2 cancer types. Because this analysis shows association rather than direction, both NPAS2-to-partner and partner-to-NPAS2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, PCNA grouped by NPAS2-low versus NPAS2-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NPAS2→partner) and Y-score (partner→NPAS2) 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
SKCMPCNA →+0.248+2.000.004.03133
UCECeIF4G →+0.209+1.874.034.04932
UCECFoxM1 →+0.169+1.523.040.00832
UCECKu80 →+0.266+1.790<.001.00132
UCECMEK1 →+0.396+2.321<.001<.00132
UCECp62 Lck ligand →+0.337+2.058.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 40 associations by consensus.

PCNA by NPAS2 expression — SKCM

Box plot of PCNA in NPAS2-low vs NPAS2-high samples in SKCM.

Explore this box plot interactively →

Exploration