FAM186B

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

Across TCGA patient cohorts, FAM186B mutation is significantly associated with the total protein of many other genes, with 51 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FAM186B-associated genes across cancer lineages are ASNS, eEF2, and eIF4E. Each is linked with FAM186B in more than 2 cancer types. Because this analysis shows association rather than direction, both FAM186B-to-partner and partner-to-FAM186B results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, ASNS grouped by FAM186B-low versus FAM186B-high in COAD.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FAM186B→partner) and Y-score (partner→FAM186B) 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
COADASNS →+0.742+3.169<.001.01833
UCECeEF2 →+0.364+1.440.003.02432
UCECeIF4E →+0.200+2.459.006<.00123
UCECGAPDH →+0.389+1.700.036.04032
UCECINPP4B →-0.223-2.321.046.00532
UCECJNK2 →+0.203+2.486.003.00932
Each partner links to its Q-omics profile. Showing the 6 strongest of 51 associations by consensus.

ASNS by FAM186B expression — COAD

Box plot of ASNS in FAM186B-low vs FAM186B-high samples in COAD.

Explore this box plot interactively →

Exploration