AP2A1

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

Across TCGA patient cohorts, AP2A1 mutation is significantly associated with the RNA expression of many other genes, with 4,912 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible AP2A1-associated genes across cancer lineages are CEP152, TRNAU1AP, and RCC1. Each is linked with AP2A1 in more than 2 cancer types. Because this analysis shows association rather than direction, both AP2A1-to-partner and partner-to-AP2A1 results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (AP2A1→partner) and Y-score (partner→AP2A1) 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
UCECCEP152 →+0.308+1.668.007.00333
COADTRNAU1AP →+0.381+3.240.005.00833
UCECRCC1 →+0.490+4.010<.001<.00133
KIRPOFD1P4Y →+0.046+7.544<.001<.00132
LGGUSP9YP10 →+0.049+7.977<.001.00732
CESCSNORD116-8 →+0.346+4.201<.001.00232
Each partner links to its Q-omics profile. Showing the 6 strongest of 4,912 associations by consensus.

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