RNF144A

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

Across TCGA patient cohorts, RNF144A mutation is significantly associated with the RNA expression of many other genes, with 2,200 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RNF144A-associated genes across cancer lineages are MIR5089, MED17, and DSG2. Each is linked with RNF144A in more than 2 cancer types. Because this analysis shows association rather than direction, both RNF144A-to-partner and partner-to-RNF144A results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MIR5089 grouped by RNF144A-low versus RNF144A-high in BLCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RNF144A→partner) and Y-score (partner→RNF144A) 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
BLCAMIR5089 →+0.574+4.719<.001.00333
UCECMED17 →+0.368+3.480.007.00233
UCECDSG2 →+0.769+2.332<.001.00333
UCECFBXO7 →+0.461+4.042<.001<.00133
UCECAAGAB →+0.521+2.042<.001.00133
UCECBLOC1S6 →+0.558+3.823<.001<.00133
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,200 associations by consensus.

MIR5089 by RNF144A expression — BLCA

Box plot of MIR5089 in RNF144A-low vs RNF144A-high samples in BLCA.

Explore this box plot interactively →

Exploration