CCIN

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

Across TCGA patient cohorts, CCIN mutation is significantly associated with the RNA expression of many other genes, with 2,614 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible CCIN-associated genes across cancer lineages are YBX1P9, RNU6ATAC42P, and MYPOP. Each is linked with CCIN in more than 2 cancer types. Because this analysis shows association rather than direction, both CCIN-to-partner and partner-to-CCIN 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 (CCIN→partner) and Y-score (partner→CCIN) 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
CESCYBX1P9 →+0.081+5.010<.001.00933
CESCRNU6ATAC42P →+0.364+5.103.009.00832
SKCMMYPOP →+0.362+3.510.002.00232
SKCMRNU6-1169P →+0.146+2.662<.001.00532
SKCMRNA5SP64 →+0.099+2.977<.001.00732
SKCMMTCO1P56 →+0.066+2.524<.001.00732
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,614 associations by consensus.

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