C1QTNF9B

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

Across TCGA cell cohorts, C1QTNF9B mutation is significantly associated with the drug of many other genes, with 22 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible C1QTNF9B-associated genes across cancer lineages are AZD7969, PLK_6522, and GSK2801. Each is linked with C1QTNF9B in more than 1 cancer types. Because this analysis shows association rather than direction, both C1QTNF9B-to-partner and partner-to-C1QTNF9B 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 (C1QTNF9B→partner) and Y-score (partner→C1QTNF9B) 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
LARGE_INTESTINEAZD7969 →+0.531+2.871.013.02131
LARGE_INTESTINEPLK_6522 →+0.697+2.871.025.02131
LARGE_INTESTINEGSK2801 →+0.338+2.871.024.02131
LARGE_INTESTINECPI-613 →+0.326+2.807.008.04431
LARGE_INTESTINEQL-XII-61 →+0.516+2.672.002.03921
LARGE_INTESTINEUNC1215 →+0.249+2.900.009.01521
Each partner links to its Q-omics profile. Showing the 6 strongest of 22 associations by consensus.

Exploration