VNN2

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

Across TCGA cell cohorts, VNN2 mutation is significantly associated with the RNA expression of many other genes, with 2 significant associations in total. CNS shows the largest number of these associations.

The most reproducible VNN2-associated genes across cancer lineages are OR6P1 and KRTAP10-7. Each is linked with VNN2 in more than 1 cancer types. Because this analysis shows association rather than direction, both VNN2-to-partner and partner-to-VNN2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, OR6P1 grouped by VNN2-low versus VNN2-high in BLOOD_Leukemia.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (VNN2→partner) and Y-score (partner→VNN2) 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_LeukemiaOR6P1 →+0.012+5.201<.001.00631
CNSKRTAP10-7 →+0.029+5.321<.001.00531
Each partner links to its Q-omics profile. Showing the 2 strongest of 2 associations by consensus.

OR6P1 by VNN2 expression — BLOOD_Leukemia

Box plot of OR6P1 in VNN2-low vs VNN2-high samples in BLOOD_Leukemia.

Explore this box plot interactively →

Exploration