FGF9

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

Across TCGA cell cohorts, FGF9 mutation is significantly associated with the RNA expression of many other genes, with 4 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible FGF9-associated genes across cancer lineages are HELT, TBC1D21, and PFN3. Each is linked with FGF9 in more than 1 cancer types. Because this analysis shows association rather than direction, both FGF9-to-partner and partner-to-FGF9 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, HELT grouped by FGF9-low versus FGF9-high in CNS.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FGF9→partner) and Y-score (partner→FGF9) 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
CNSHELT →+0.041+5.321<.001.00531
LARGE_INTESTINETBC1D21 →+0.015+5.022<.001.00231
LARGE_INTESTINEPFN3 →+0.169+4.467<.001.00431
LARGE_INTESTINEPYDC2 →+0.108+4.415<.001.00731
Each partner links to its Q-omics profile. Showing the 4 strongest of 4 associations by consensus.

HELT by FGF9 expression — CNS

Box plot of HELT in FGF9-low vs FGF9-high samples in CNS.

Explore this box plot interactively →

Exploration