PHF19

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

Across TCGA patient cohorts, PHF19 mutation is significantly associated with the RNA expression of many other genes, with 3,817 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PHF19-associated genes across cancer lineages are VTRNA2-2P, RNU6-1089P, and LINC02210-CRHR1. Each is linked with PHF19 in more than 1 cancer types. Because this analysis shows association rather than direction, both PHF19-to-partner and partner-to-PHF19 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, VTRNA2-2P grouped by PHF19-low versus PHF19-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PHF19→partner) and Y-score (partner→PHF19) 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
SKCMVTRNA2-2P →+0.534+3.953<.001.00532
SKCMRNU6-1089P →+0.412+5.356<.001<.00132
SKCMLINC02210-CRHR1 →+0.145+3.838<.001.00632
UCECIGHD2-2 →+0.879+1.872.007<.00132
UCECSNORD90 →+0.205+1.814.002.00732
UCECRNA5SP408 →+0.241+2.450.001.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,817 associations by consensus.

VTRNA2-2P by PHF19 expression — SKCM

Box plot of VTRNA2-2P in PHF19-low vs PHF19-high samples in SKCM.

Explore this box plot interactively →

Exploration