NHLRC2

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

Across TCGA patient cohorts, NHLRC2 mutation is significantly associated with the total protein of many other genes, with 28 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NHLRC2-associated genes across cancer lineages are 4E-BP1, EGFR_pY1068, and IGFBP2. Each is linked with NHLRC2 in more than 1 cancer types. Because this analysis shows association rather than direction, both NHLRC2-to-partner and partner-to-NHLRC2 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 (NHLRC2→partner) and Y-score (partner→NHLRC2) 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
UCEC4E-BP1 →+0.293+2.584.003.01032
UCECEGFR_pY1068 →-0.220-1.874.019.04931
UCECIGFBP2 →-0.849-2.169<.001.00331
UCECJNK2 →+0.246+2.169<.001.00331
UCECKu80 →+0.242+1.778.006.00831
UCECMAPK_pT202_Y204 →-0.384-2.000.029.03031
Each partner links to its Q-omics profile. Showing the 6 strongest of 28 associations by consensus.

Exploration