SSR2

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

Across TCGA patient cohorts, SSR2 mutation is significantly associated with the total protein of many other genes, with 3 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SSR2-associated genes across cancer lineages are p21, p27, and XBP1. Each is linked with SSR2 in more than 1 cancer types. Because this analysis shows association rather than direction, both SSR2-to-partner and partner-to-SSR2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, p21 grouped by SSR2-low versus SSR2-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SSR2→partner) and Y-score (partner→SSR2) 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
UCECp21 →+0.226+2.321.019.03531
UCECp27 →+0.291+3.169.007.01931
UCECXBP1 →-0.231-3.000.001.03621
Each partner links to its Q-omics profile. Showing the 3 strongest of 3 associations by consensus.

p21 by SSR2 expression — UCEC

Box plot of p21 in SSR2-low vs SSR2-high samples in UCEC.

Explore this box plot interactively →

Exploration