NRIP3

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

Across TCGA cell cohorts, NRIP3 mutation is significantly associated with the mutation status of many other genes, with 1,007 significant associations in total. BLOOD_Leukemia shows the largest number of these associations.

The most reproducible NRIP3-associated genes across cancer lineages are DMTF1, PARP6, and OR4D6. Each is linked with NRIP3 in more than 2 cancer types. Because this analysis shows association rather than direction, both NRIP3-to-partner and partner-to-NRIP3 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, DMTF1 grouped by NRIP3-low versus NRIP3-high in BLOOD_Leukemia.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NRIP3→partner) and Y-score (partner→NRIP3) 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
BLOOD_LeukemiaDMTF1 →+4.309+4.560.007.00713
BLOOD_LeukemiaPARP6 →+4.894+4.894.004.00413
BLOOD_LeukemiaOR4D6 →+4.894+4.894.004.00412
BLOOD_LeukemiaMARS1 →+3.309+4.794.002.00212
BLOOD_LeukemiaSF1 →+3.479+4.932.002.00212
BLOOD_LeukemiaETFDH →+4.894+4.894.004.00412
Each partner links to its Q-omics profile. Showing the 6 strongest of 1,007 associations by consensus.

DMTF1 by NRIP3 expression — BLOOD_Leukemia

Box plot of DMTF1 in NRIP3-low vs NRIP3-high samples in BLOOD_Leukemia.

Explore this box plot interactively →

Exploration