FPGS

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

Across TCGA patient cohorts, FPGS mutation is significantly associated with the RNA expression of many other genes, with 428 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FPGS-associated genes across cancer lineages are LINC00351, NOCT, and CHAF1A. Each is linked with FPGS in more than 1 cancer types. Because this analysis shows association rather than direction, both FPGS-to-partner and partner-to-FPGS results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, LINC00351 grouped by FPGS-low versus FPGS-high in CESC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FPGS→partner) and Y-score (partner→FPGS) 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
CESCLINC00351 →+0.162+5.201<.001.00732
UCECNOCT →+0.652+2.233.001.00632
UCECCHAF1A →+0.551+2.243.006.00632
UCECCXCR6 →+0.832+2.917<.001.00132
UCECTXLNA →+0.342+2.732.008.00332
LGGMIR582 →+0.663+6.787<.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 428 associations by consensus.

LINC00351 by FPGS expression — CESC

Box plot of LINC00351 in FPGS-low vs FPGS-high samples in CESC.

Explore this box plot interactively →

Exploration