GPR89B

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

Across TCGA patient cohorts, GPR89B mutation is significantly associated with the RNA expression of many other genes, with 2,680 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible GPR89B-associated genes across cancer lineages are RNA5SP412, GOLGA8CP, and RNU6-1169P. Each is linked with GPR89B in more than 2 cancer types. Because this analysis shows association rather than direction, both GPR89B-to-partner and partner-to-GPR89B results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (GPR89B→partner) and Y-score (partner→GPR89B) 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
UCECRNA5SP412 →+0.706+1.867<.001.00733
SKCMGOLGA8CP →+0.008+3.533<.001.00732
SKCMRNU6-1169P →+0.389+4.362<.001.00132
SKCMHDAC9-AS1 →+0.189+4.159<.001.00232
UCECMIR193A →+0.566+2.077.001.00132
UCECTRAV10 →+0.399+2.684.001<.00132
Each partner links to its Q-omics profile. Showing the 6 strongest of 2,680 associations by consensus.

Exploration