QRFPR

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

Across TCGA patient cohorts, QRFPR mutation is significantly associated with the total protein of many other genes, with 26 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible QRFPR-associated genes across cancer lineages are eIF4E, INPP4B, and Notch1. Each is linked with QRFPR in more than 1 cancer types. Because this analysis shows association rather than direction, both QRFPR-to-partner and partner-to-QRFPR 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 (QRFPR→partner) and Y-score (partner→QRFPR) 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
UCECeIF4E →+0.162+2.335.033.01832
UCECINPP4B →-0.349-2.415.002.00332
UCECNotch1 →+0.118+2.232.020.00532
UCECCaspase-7-cleavedD198 →+0.572+2.341.007.00332
UCEC14-3-3_beta →-0.081-2.295.024.03331
UCECEGFR_pY1068 →-0.234-2.459.009.01831
Each partner links to its Q-omics profile. Showing the 6 strongest of 26 associations by consensus.

Exploration