GPRIN1

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

Across TCGA patient cohorts, GPRIN1 mutation is significantly associated with the RNA expression of many other genes, with 3,899 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible GPRIN1-associated genes across cancer lineages are RNU1-17P, DUTP3, and LINC02794. Each is linked with GPRIN1 in more than 3 cancer types. Because this analysis shows association rather than direction, both GPRIN1-to-partner and partner-to-GPRIN1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNU1-17P grouped by GPRIN1-low versus GPRIN1-high in UCEC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (GPRIN1→partner) and Y-score (partner→GPRIN1) 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
UCECRNU1-17P →+0.132+1.935.004.00634
SARCDUTP3 →+0.121+4.778<.001.00634
LGGLINC02794 →+0.065+4.711<.001.00333
CESCMED15P6 →+0.446+5.786<.001<.00132
CESCNF1P10 →+0.362+5.569<.001.00232
UCECNDUFAF2 →+0.492+2.000<.001.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,899 associations by consensus.

RNU1-17P by GPRIN1 expression — UCEC

Box plot of RNU1-17P in GPRIN1-low vs GPRIN1-high samples in UCEC.

Explore this box plot interactively →

Exploration