FEM1A

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

Across TCGA patient cohorts, FEM1A mutation is significantly associated with the RNA expression of many other genes, with 957 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FEM1A-associated genes across cancer lineages are RN7SL717P, ACD, and SUGT1P4. Each is linked with FEM1A in more than 1 cancer types. Because this analysis shows association rather than direction, both FEM1A-to-partner and partner-to-FEM1A results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SL717P grouped by FEM1A-low versus FEM1A-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FEM1A→partner) and Y-score (partner→FEM1A) 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
SKCMRN7SL717P →+0.058+3.362.001.00632
UCECACD →+0.439+2.436<.001.00132
LUSCSUGT1P4 →+0.192+5.578<.001.00232
COADREXO1L8P →+0.015+4.142<.001.00632
UCECMEIG1 →-0.481-2.297.004.00632
UCECRNU6-222P →+0.526+2.376<.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 957 associations by consensus.

RN7SL717P by FEM1A expression — SKCM

Box plot of RN7SL717P in FEM1A-low vs FEM1A-high samples in SKCM.

Explore this box plot interactively →

Exploration