ASB12

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

Across TCGA patient cohorts, ASB12 mutation is significantly associated with the RNA expression of many other genes, with 1,313 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible ASB12-associated genes across cancer lineages are FAM47DP, PINCR, and BNIP3P2. Each is linked with ASB12 in more than 1 cancer types. Because this analysis shows association rather than direction, both ASB12-to-partner and partner-to-ASB12 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 (ASB12→partner) and Y-score (partner→ASB12) 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
READFAM47DP →+0.024+3.855.004.00832
READPINCR →+0.192+4.142<.001.00432
READBNIP3P2 →+0.448+4.179<.001.00332
READBNIP3P6 →+0.284+4.341<.001.00732
LGGKRTAP20-3 →+0.174+7.977<.001.00732
LGGRNU6-1211P →+0.388+7.977<.001.00732
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,313 associations by consensus.

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