MIR487A

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

Across TCGA patient cohorts, MIR487A mutation is significantly associated with the RNA expression of many other genes, with 34 significant associations in total. STAD shows the largest number of these associations.

The most reproducible MIR487A-associated genes across cancer lineages are NPS, RNU6-839P, and LINC02509. Each is linked with MIR487A in more than 1 cancer types. Because this analysis shows association rather than direction, both MIR487A-to-partner and partner-to-MIR487A 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 (MIR487A→partner) and Y-score (partner→MIR487A) 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
UCECNPS →+0.344+6.722<.001<.00132
STADRNU6-839P →+0.451+5.274<.001.00632
STADLINC02509 →+0.091+5.274.001.00632
SKCMMTCO3P41 →+0.190+6.080<.001.00231
SKCMOR7E53P →+0.115+5.292<.001.00631
SKCMRNU6-1183P →+0.730+5.594<.001.00431
Each partner links to its Q-omics profile. Showing the 6 strongest of 34 associations by consensus.

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