PPP1R2C

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

Across TCGA patient cohorts, PPP1R2C RNA expression is significantly associated with the go_rna of many other GO terms, with 6,023 significant associations in total. STAD shows the largest number of these associations.

The most reproducible PPP1R2C-associated GO terms across cancer lineages are Positive regulation of lymphocyte differentiation, Negative regulation of immune response, and Granzyme-mediated programmed cell death signaling pathway. Each is linked with PPP1R2C in more than 11 cancer types. Because this analysis shows association rather than direction, both PPP1R2C-to-partner and partner-to-PPP1R2C results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Positive regulation of lymphocyte differentiation grouped by PPP1R2C-low versus PPP1R2C-high in STAD.

RNA expression associated GO terms by consensus

Ranked by combined sampling and lineage consensus. X-score (PPP1R2C→partner) and Y-score (partner→PPP1R2C) 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
STADPositive regulation of lymphocyte differentiation →+0.075+0.056<.001<.001312
STADNegative regulation of immune response →+0.070+0.066<.001<.001312
TGCTGranzyme-mediated programmed cell death signaling pathway →+0.114+1.228<.001<.001311
STADRegulation of leukocyte migration →+0.060+0.083<.001<.001311
STADResponse to type II interferon →+0.076+0.051<.001<.001311
STADResponse to tumor necrosis factor →+0.063+0.100<.001<.001311
Each partner links to its Q-omics profile. Showing the 6 strongest of 6,023 associations by consensus.

Positive regulation of lymphocyte differentiation by PPP1R2C expression — STAD

Box plot of Positive regulation of lymphocyte differentiation in PPP1R2C-low vs PPP1R2C-high samples in STAD.

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