RIN1

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

Across TCGA patient cohorts, RIN1 mutation is significantly associated with the RNA expression of many other genes, with 3,722 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RIN1-associated genes across cancer lineages are GUSBP17, HNRNPA3P8, and OR7A8P. Each is linked with RIN1 in more than 1 cancer types. Because this analysis shows association rather than direction, both RIN1-to-partner and partner-to-RIN1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, GUSBP17 grouped by RIN1-low versus RIN1-high in SKCM.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RIN1→partner) and Y-score (partner→RIN1) 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
SKCMGUSBP17 →+0.117+2.866.004.00132
SKCMHNRNPA3P8 →+0.054+2.396.008.00932
CESCOR7A8P →+0.064+3.760.001.00732
BRCAMTHFD2P3 →+0.180+4.760<.001.00732
UCECLINC00624 →+0.354+2.173.003.00232
UCECMAPRE1 →+0.416+1.818.005.00232
Each partner links to its Q-omics profile. Showing the 6 strongest of 3,722 associations by consensus.

GUSBP17 by RIN1 expression — SKCM

Box plot of GUSBP17 in RIN1-low vs RIN1-high samples in SKCM.

Explore this box plot interactively →

Exploration