FA2H

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

Across TCGA patient cohorts, FA2H mutation is significantly associated with the RNA expression of many other genes, with 704 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible FA2H-associated genes across cancer lineages are RN7SKP286, HMGN2P26, and RN7SL553P. Each is linked with FA2H in more than 1 cancer types. Because this analysis shows association rather than direction, both FA2H-to-partner and partner-to-FA2H results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SKP286 grouped by FA2H-low versus FA2H-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (FA2H→partner) and Y-score (partner→FA2H) 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
SKCMRN7SKP286 →+0.096+6.225<.001<.00132
UCECHMGN2P26 →+0.108+2.814.001.00132
KIRPRN7SL553P →+0.160+6.528<.001.00132
UCECTRBV7-9 →+0.686+2.593.008.00631
UCECTMEM150B →+0.546+2.425.003.00231
UCECCCDC43 →+0.440+2.447.009.00131
Each partner links to its Q-omics profile. Showing the 6 strongest of 704 associations by consensus.

RN7SKP286 by FA2H expression — SKCM

Box plot of RN7SKP286 in FA2H-low vs FA2H-high samples in SKCM.

Explore this box plot interactively →

Exploration