PFKL

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

Across TCGA patient cohorts, PFKL mutation is significantly associated with the total protein of many other genes, with 45 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible PFKL-associated genes across cancer lineages are eIF4E, FoxM1, and MSH2. Each is linked with PFKL in more than 1 cancer types. Because this analysis shows association rather than direction, both PFKL-to-partner and partner-to-PFKL results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, eIF4E grouped by PFKL-low versus PFKL-high in COAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PFKL→partner) and Y-score (partner→PFKL) 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
COADeIF4E →+0.265+2.820.001.03532
UCECFoxM1 →+0.200+1.736.026.00732
UCECMSH2 →-0.164-2.295.040.03332
UCECPCNA →+0.231+3.000.002<.00132
UCECATM →-0.385-1.440.014.02432
COADp38-MAPK →+0.201+3.169.014.01832
Each partner links to its Q-omics profile. Showing the 6 strongest of 45 associations by consensus.

eIF4E by PFKL expression — COAD

Box plot of eIF4E in PFKL-low vs PFKL-high samples in COAD.

Explore this box plot interactively →

Exploration