ANKRD42

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

Across TCGA patient cohorts, ANKRD42 mutation is significantly associated with the RNA expression of many other genes, with 2,533 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible ANKRD42-associated genes across cancer lineages are RN7SL66P, MIR4769, and SNX3P1Y. Each is linked with ANKRD42 in more than 2 cancer types. Because this analysis shows association rather than direction, both ANKRD42-to-partner and partner-to-ANKRD42 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SL66P grouped by ANKRD42-low versus ANKRD42-high in READ.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (ANKRD42→partner) and Y-score (partner→ANKRD42) 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
READRN7SL66P →+0.177+5.925<.001.00233
CESCMIR4769 →+0.402+5.579<.001.00132
UCECSNX3P1Y →+0.056+3.620<.001.00932
READMIR887 →+0.370+5.925<.001.00232
UCECC19orf47 →+0.308+3.818.005<.00132
UCECLRRC71 →-1.157-3.896<.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,533 associations by consensus.

RN7SL66P by ANKRD42 expression — READ

Box plot of RN7SL66P in ANKRD42-low vs ANKRD42-high samples in READ.

Explore this box plot interactively →

Exploration