C15orf32

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

Across TCGA patient cohorts, C15orf32 mutation is significantly associated with the RNA expression of many other genes, with 48 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible C15orf32-associated genes across cancer lineages are OR7E46P, MTND1P33, and LINC01056. Each is linked with C15orf32 in more than 1 cancer types. Because this analysis shows association rather than direction, both C15orf32-to-partner and partner-to-C15orf32 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 (C15orf32→partner) and Y-score (partner→C15orf32) 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
SKCMOR7E46P →+0.046+3.953<.001.00531
SKCMMTND1P33 →+0.040+5.039<.001.00331
SKCMLINC01056 →+0.577+4.034<.001.00431
SKCMOR9A1P →+0.064+3.953<.001.00531
SKCMLINC02096 →+0.070+4.163<.001.00331
SKCMRN7SL681P →+0.254+3.993<.001.00531
Each partner links to its Q-omics profile. Showing the 6 strongest of 48 associations by consensus.

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