FAM32A

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

Across TCGA patient cohorts, FAM32A mutation is significantly associated with the RNA expression of many other genes, with 3 significant associations in total. COAD shows the largest number of these associations.

The most reproducible FAM32A-associated genes across cancer lineages are SDR42E1P4, RNU6-694P, and RN7SL93P. Each is linked with FAM32A in more than 1 cancer types. Because this analysis shows association rather than direction, both FAM32A-to-partner and partner-to-FAM32A results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SDR42E1P4 grouped by FAM32A-low versus FAM32A-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FAM32A→partner) and Y-score (partner→FAM32A) 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
UCECSDR42E1P4 →+0.199+8.066<.001.00731
COADRNU6-694P →+0.610+5.893<.001.00231
COADRN7SL93P →+0.467+5.145<.001.00731
Each partner links to its Q-omics profile. Showing the 3 strongest of 3 associations by consensus.

SDR42E1P4 by FAM32A expression — UCEC

Box plot of SDR42E1P4 in FAM32A-low vs FAM32A-high samples in UCEC.

Explore this box plot interactively →

Exploration