SCRN1

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

Across TCGA patient cohorts, SCRN1 mutation is significantly associated with the RNA expression of many other genes, with 2,157 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SCRN1-associated genes across cancer lineages are MIR7-3, SOSTDC1, and RGS1. Each is linked with SCRN1 in more than 1 cancer types. Because this analysis shows association rather than direction, both SCRN1-to-partner and partner-to-SCRN1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, MIR7-3 grouped by SCRN1-low versus SCRN1-high in CESC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (SCRN1→partner) and Y-score (partner→SCRN1) 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
CESCMIR7-3 →+0.218+4.757<.001.00432
UCECSOSTDC1 →-0.781-2.239.006.00132
UCECRGS1 →+0.635+2.354.008.00332
UCECCBARP →+0.629+2.269<.001<.00132
UCECHCN2 →+0.347+1.410.005.00532
BRCACGB1 →+0.039+8.471<.001.00532
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,157 associations by consensus.

MIR7-3 by SCRN1 expression — CESC

Box plot of MIR7-3 in SCRN1-low vs SCRN1-high samples in CESC.

Explore this box plot interactively →

Exploration