RANBP17

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

Across TCGA patient cohorts, RANBP17 mutation is significantly associated with the RNA expression of many other genes, with 5,060 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RANBP17-associated genes across cancer lineages are TMEM269, MIR5002, and EIF4A1P12. Each is linked with RANBP17 in more than 3 cancer types. Because this analysis shows association rather than direction, both RANBP17-to-partner and partner-to-RANBP17 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 (RANBP17→partner) and Y-score (partner→RANBP17) 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
UCECTMEM269 →+0.140+1.327<.001.00634
ACCMIR5002 →+0.500+6.266<.001<.00133
READEIF4A1P12 →+1.127+5.039<.001.00833
SKCMTHOC5 →+0.408+2.725.003.00233
SKCMHSDL1 →+0.391+2.360.008.00233
SKCMPHF7 →+0.397+2.372.001.00233
Each partner links to its Q-omics profile. Showing the 6 strongest of 5,060 associations by consensus.

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