PHF2

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

Across TCGA patient cohorts, PHF2 mutation is significantly associated with the RNA expression of many other genes, with 4,561 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PHF2-associated genes across cancer lineages are COX15, SSTR5, and BOLA3. Each is linked with PHF2 in more than 2 cancer types. Because this analysis shows association rather than direction, both PHF2-to-partner and partner-to-PHF2 results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PHF2→partner) and Y-score (partner→PHF2) 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
UCECCOX15 →+0.424+2.638<.001<.00133
UCECSSTR5 →+0.360+1.360<.001.00233
UCECBOLA3 →+0.282+1.463.003.00533
UCECHSPA4L →+0.690+2.258<.001<.00133
COADIFI27L1 →+0.632+2.807<.001.00333
UCECPBK →+0.868+1.818<.001<.00133
Each partner links to its Q-omics profile. Showing the 6 strongest of 4,561 associations by consensus.

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