Regulation of G2/MI transition of meiotic cell cycle

pathway activity — cross-omics
GO:0110030Cross-omicsRNA → PROTEIN-MSPatientPairwise association · TCGA cohorts

Across TCGA patient cohorts, RNA activity of the Regulation of G2/MI transition of meiotic cell cycle pathway is significantly associated with the protein abundance of multiple proteins, with the LSCC cohort showing a particularly strong set of associations.

The most reproducible pathway-associated proteins across cancer lineages are RFC2, RFC4, and RPL12_S38, each associated with the pathway in up to 10 cancer types. Since the analysis shows associations rather than directional relationships, both pathway-to-partner and partner-to-pathway views are reported.

Each partner is linked to its corresponding Q-omics profile. The scatter plot shows the strongest association, Regulation of G2/MI transition of meiotic cell cycle activity versus RFC2 in LSCC (Pearson r = 0.74).

Pathway-associated proteins by consensus

Ranked by combined sampling and lineage consensus. X-score (pathway→partner) and Y-score (partner→pathway) are standardized regression coefficients; both directions are reported because the association is undirected. The reported p-values are derived from the association test.
LineagePartner proteinX-scoreY-scorep(X)p(Y)Sampling consensusLineage consensus
LSCCRFC2 →+0.500+0.125<.001<.001310
LSCCRFC4 →+0.547+0.115<.001<.001310
LUADRPL12_S38 →+1.186+0.119<.001<.001310
BRCARRM1 →+0.581+0.098<.001<.001310
UCECRRM2 →+0.929+0.242<.001.002310
LUADATAD2_S342 →+1.318+0.110<.001<.001310
Each partner links to its Q-omics profile. Showing the 6 strongest associations by consensus.

GO:0110030 vs RFC2 — LSCC

Per-sample scatter of Regulation of G2/MI transition of meiotic cell cycle activity vs RFC2 in LSCC.

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Exploration