PRSS22

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

Across TCGA cell cohorts, PRSS22 mutation is significantly associated with the mutation status of many other genes, with 5,023 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible PRSS22-associated genes across cancer lineages are SYNC, RASGEF1A, and TCF20. Each is linked with PRSS22 in more than 3 cancer types. Because this analysis shows association rather than direction, both PRSS22-to-partner and partner-to-PRSS22 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, SYNC grouped by PRSS22-low versus PRSS22-high in BLOOD_Leukemia.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PRSS22→partner) and Y-score (partner→PRSS22) 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
BLOOD_LeukemiaSYNC →+6.321+6.321.001.00114
OVARYRASGEF1A →+4.977+4.415.007.00714
OVARYTCF20 →+3.240+4.467.004.00413
OVARYTRMU →+4.977+4.415.007.00713
OVARYGMEB2 →+4.977+4.415.007.00713
OVARYJAG1 →+4.562+5.217<.001<.00113
Each partner links to its Q-omics profile. Showing the 6 strongest of 5,023 associations by consensus.

SYNC by PRSS22 expression — BLOOD_Leukemia

Box plot of SYNC in PRSS22-low vs PRSS22-high samples in BLOOD_Leukemia.

Explore this box plot interactively →

Exploration