PHF8

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

Across TCGA cell cohorts, PHF8 mutation is significantly associated with the RNA expression of many other genes, with 12 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible PHF8-associated genes across cancer lineages are FGF3, OR51T1, and GSG1L2. Each is linked with PHF8 in more than 1 cancer types. Because this analysis shows association rather than direction, both PHF8-to-partner and partner-to-PHF8 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, FGF3 grouped by PHF8-low versus PHF8-high in CNS.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PHF8→partner) and Y-score (partner→PHF8) 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
CNSFGF3 →+0.081+4.981<.001.00831
BLOOD_LeukemiaOR51T1 →+0.071+4.922<.001.00931
BLOOD_LeukemiaGSG1L2 →+0.058+5.969<.001.00131
LUNG_NSCLC_LUADOR7G1 →+0.017+5.266<.001.00131
LARGE_INTESTINEASPN →+0.056+3.841<.001<.00131
LARGE_INTESTINEACER1 →+0.069+2.823.003.00231
Each partner links to its Q-omics profile. Showing the 6 strongest of 12 associations by consensus.

FGF3 by PHF8 expression — CNS

Box plot of FGF3 in PHF8-low vs PHF8-high samples in CNS.

Explore this box plot interactively →

Exploration