NMNAT2

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

Across TCGA cell cohorts, NMNAT2 mutation is significantly associated with the RNA expression of many other genes, with 4 significant associations in total. BLOOD_Lymphoma shows the largest number of these associations.

The most reproducible NMNAT2-associated genes across cancer lineages are PRSS54, SMCP, and C11orf97. Each is linked with NMNAT2 in more than 1 cancer types. Because this analysis shows association rather than direction, both NMNAT2-to-partner and partner-to-NMNAT2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, PRSS54 grouped by NMNAT2-low versus NMNAT2-high in BLOOD_Lymphoma.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NMNAT2→partner) and Y-score (partner→NMNAT2) 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_LymphomaPRSS54 →+0.046+4.867<.001.00931
BLOOD_LymphomaSMCP →+0.034+4.867<.001.00931
BLOOD_LymphomaC11orf97 →+2.118+5.209<.001.00531
LARGE_INTESTINECD300H →+0.039+4.415<.001.00731
Each partner links to its Q-omics profile. Showing the 4 strongest of 4 associations by consensus.

PRSS54 by NMNAT2 expression — BLOOD_Lymphoma

Box plot of PRSS54 in NMNAT2-low vs NMNAT2-high samples in BLOOD_Lymphoma.

Explore this box plot interactively →

Exploration