S1PR2

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

Across TCGA patient cohorts, S1PR2 mutation is significantly associated with the immune_cell of many other genes, with 3 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible S1PR2-associated genes across cancer lineages are Eosinophils, CMP, and Plasma cells. Each is linked with S1PR2 in more than 2 cancer types. Because this analysis shows association rather than direction, both S1PR2-to-partner and partner-to-S1PR2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, Eosinophils grouped by S1PR2-low versus S1PR2-high in LUSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (S1PR2→partner) and Y-score (partner→S1PR2) 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
LUSCEosinophils →+0.054+3.173<.001.04933
STADCMP →+0.048+3.413<.001.03431
UCECPlasma cells →-0.021-3.034.040.02031
Each partner links to its Q-omics profile. Showing the 3 strongest of 3 associations by consensus.

Eosinophils by S1PR2 expression — LUSC

Box plot of Eosinophils in S1PR2-low vs S1PR2-high samples in LUSC.

Explore this box plot interactively →

Exploration