RINT1

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

Across TCGA patient cohorts, RINT1 mutation is significantly associated with the RNA expression of many other genes, with 1,291 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible RINT1-associated genes across cancer lineages are RN7SL627P, MIR8053, and ZSWIM5P1. Each is linked with RINT1 in more than 2 cancer types. Because this analysis shows association rather than direction, both RINT1-to-partner and partner-to-RINT1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RN7SL627P grouped by RINT1-low versus RINT1-high in BLCA.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RINT1→partner) and Y-score (partner→RINT1) 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
BLCARN7SL627P →+0.096+4.618.002.00533
SKCMMIR8053 →+0.266+4.328<.001.00733
BLCAZSWIM5P1 →+0.012+4.147<.001.00932
BLCATRIM51EP →+0.077+4.106<.001.00232
BLCAWRBP1 →+0.153+3.317.002.00832
HNSCRN7SKP120 →+0.056+5.626<.001.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,291 associations by consensus.

RN7SL627P by RINT1 expression — BLCA

Box plot of RN7SL627P in RINT1-low vs RINT1-high samples in BLCA.

Explore this box plot interactively →

Exploration