IRF8

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

Across TCGA patient cohorts, IRF8 mutation is significantly associated with the RNA expression of many other genes, with 1,999 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible IRF8-associated genes across cancer lineages are CENPH, FGD5, and EME1. Each is linked with IRF8 in more than 2 cancer types. Because this analysis shows association rather than direction, both IRF8-to-partner and partner-to-IRF8 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, CENPH grouped by IRF8-low versus IRF8-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (IRF8→partner) and Y-score (partner→IRF8) 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
SKCMCENPH →+0.585+1.925.004.00932
UCECFGD5 →-0.551-2.486.002.00132
UCECEME1 →+0.527+1.949.001.00132
UCECFANCC →+0.369+2.032.003.00432
UCECCHAF1B →+0.641+2.643<.001<.00132
UCECNAE1 →+0.440+1.652.002.00632
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,999 associations by consensus.

CENPH by IRF8 expression — SKCM

Box plot of CENPH in IRF8-low vs IRF8-high samples in SKCM.

Explore this box plot interactively →

Exploration