FEM1B

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

Across TCGA patient cohorts, FEM1B mutation is significantly associated with the RNA expression of many other genes, with 2,084 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FEM1B-associated genes across cancer lineages are MIR6085, RNY4P16, and SCGB1C1. Each is linked with FEM1B in more than 1 cancer types. Because this analysis shows association rather than direction, both FEM1B-to-partner and partner-to-FEM1B results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MIR6085 grouped by FEM1B-low versus FEM1B-high in LUAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FEM1B→partner) and Y-score (partner→FEM1B) 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
LUADMIR6085 →+0.444+3.659<.001.00932
LUSCRNY4P16 →+0.377+5.148<.001.00232
STADSCGB1C1 →+0.187+4.005<.001.00632
UCECMTATP6P21 →+0.286+2.060<.001.00232
COADEZHIP →+0.677+3.387<.001.00731
COADLCE1C →+0.169+4.246.003<.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,084 associations by consensus.

MIR6085 by FEM1B expression — LUAD

Box plot of MIR6085 in FEM1B-low vs FEM1B-high samples in LUAD.

Explore this box plot interactively →

Exploration