PLEKHF1

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

Across TCGA cell cohorts, PLEKHF1 mutation is significantly associated with the RNA expression of many other genes, with 129 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible PLEKHF1-associated genes across cancer lineages are CST5, CYLC1, and FAM205C. Each is linked with PLEKHF1 in more than 1 cancer types. Because this analysis shows association rather than direction, both PLEKHF1-to-partner and partner-to-PLEKHF1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, CST5 grouped by PLEKHF1-low versus PLEKHF1-high in CNS.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PLEKHF1→partner) and Y-score (partner→PLEKHF1) 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
CNSCST5 →+0.134+4.981<.001.00832
CNSCYLC1 →+0.013+5.321<.001.00531
CNSFAM205C →+0.043+4.981<.001.00831
LARGE_INTESTINERAB3A →+0.759+3.451.008.00231
LARGE_INTESTINESH3GL2 →+1.483+3.837<.001<.00131
LARGE_INTESTINEATP5PB →+0.513+3.364.001.00231
Each partner links to its Q-omics profile. Showing the 6 strongest of 129 associations by consensus.

CST5 by PLEKHF1 expression — CNS

Box plot of CST5 in PLEKHF1-low vs PLEKHF1-high samples in CNS.

Explore this box plot interactively →

Exploration