CCDC141

RNA expression — cross-omics
Cross-omicsRNA → FUNCTION-RNACell-linePairwise association · TCGA cohorts

Across TCGA cell cohorts, CCDC141 RNA expression is significantly associated with the go_rna of many other GO terms, with 2,365 significant associations in total. SOFT_TISSUE shows the largest number of these associations.

The most reproducible CCDC141-associated GO terms across cancer lineages are Mitotic cell cycle phase transition, Meiotic sister chromatid cohesion, centromeric, and DNA replication-dependent chromatin disassembly. Each is linked with CCDC141 in more than 4 cancer types. Because this analysis shows association rather than direction, both CCDC141-to-partner and partner-to-CCDC141 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Mitotic cell cycle phase transition grouped by CCDC141-low versus CCDC141-high in SOFT_TISSUE.

RNA expression associated GO terms by consensus

Ranked by combined sampling and lineage consensus. X-score (CCDC141→partner) and Y-score (partner→CCDC141) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.
LineagePartner GO termX-scoreY-scorep(X)p(Y)Sampling consensusLineage consensus
SOFT_TISSUEMitotic cell cycle phase transition →+0.059+0.874<.001.00335
BLOOD_MyelomaMeiotic sister chromatid cohesion, centromeric →+0.102+0.623.002.00635
SOFT_TISSUEDNA replication-dependent chromatin disassembly →+0.109+1.229<.001<.00135
SOFT_TISSUEProtein deubiquitination →+0.048+0.962<.001.00735
SOFT_TISSUERegulation of binding of sperm to zona pellucida →-0.741-0.960.004.00135
SOFT_TISSUERegulation of nucleotide-excision repair →+0.058+0.818.005.00535
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,365 associations by consensus.

Mitotic cell cycle phase transition by CCDC141 expression — SOFT_TISSUE

Box plot of Mitotic cell cycle phase transition in CCDC141-low vs CCDC141-high samples in SOFT_TISSUE.

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