PNISR

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

Across TCGA cell cohorts, PNISR mutation is significantly associated with the RNA expression of many other genes, with 27 significant associations in total. BLOOD_Leukemia shows the largest number of these associations.

The most reproducible PNISR-associated genes across cancer lineages are NCMAP, CHRNA2, and SPACA5. Each is linked with PNISR in more than 1 cancer types. Because this analysis shows association rather than direction, both PNISR-to-partner and partner-to-PNISR results are reported.

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

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (PNISR→partner) and Y-score (partner→PNISR) 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
SOFT_TISSUENCMAP →+0.303+4.554<.001<.00132
SOFT_TISSUECHRNA2 →+0.106+3.999.009.00431
SOFT_TISSUESPACA5 →+0.965+4.142.002.00331
SOFT_TISSUEFADS6 →+0.185+3.684<.001.00931
BLOOD_LeukemiaEPPIN →+0.006+5.507<.001<.00131
BLOOD_LeukemiaADRA1A →+0.375+4.705<.001.00331
Each partner links to its Q-omics profile. Showing the 6 strongest of 27 associations by consensus.

NCMAP by PNISR expression — SOFT_TISSUE

Box plot of NCMAP in PNISR-low vs PNISR-high samples in SOFT_TISSUE.

Explore this box plot interactively →

Exploration