PHF8

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

Across TCGA patient cohorts, PHF8 mutation is significantly associated with the RNA expression of many other genes, with 4,238 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PHF8-associated genes across cancer lineages are RNA5SP411, RNVU1-28, and SFXN1. Each is linked with PHF8 in more than 2 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, RNA5SP411 grouped by PHF8-low versus PHF8-high in UCEC.

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
UCECRNA5SP411 →+0.480+1.159.004.00633
UCECRNVU1-28 →+0.532+1.686<.001<.00133
UCECSFXN1 →+0.422+1.357<.001<.00133
UCECCOX10 →+0.354+1.485<.001<.00133
UCECELAC2 →+0.354+1.618<.001<.00133
LUADMIR3922 →+0.368+3.864.003.00333
Each partner links to its Q-omics profile. Showing the 6 strongest of 4,238 associations by consensus.

RNA5SP411 by PHF8 expression — UCEC

Box plot of RNA5SP411 in PHF8-low vs PHF8-high samples in UCEC.

Explore this box plot interactively →

Exploration