RFTN2

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

Across TCGA cell cohorts, RFTN2 mutation is significantly associated with the RNA expression of many other genes, with 6 significant associations in total. BLOOD_Lymphoma shows the largest number of these associations.

The most reproducible RFTN2-associated genes across cancer lineages are ARMH2, KRT71, and HES3. Each is linked with RFTN2 in more than 1 cancer types. Because this analysis shows association rather than direction, both RFTN2-to-partner and partner-to-RFTN2 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, ARMH2 grouped by RFTN2-low versus RFTN2-high in SOFT_TISSUE.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (RFTN2→partner) and Y-score (partner→RFTN2) 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_TISSUEARMH2 →+0.040+4.930.001.00831
BLOOD_LymphomaKRT71 →+0.009+4.643<.001.00531
BLOOD_LymphomaHES3 →+0.133+4.523<.001.00431
BLOOD_LymphomaSHOX →+0.031+4.523<.001.00431
LARGE_INTESTINEBRDT →+0.122+3.906<.001.00231
LARGE_INTESTINECCDC195 →+0.037+3.297.001.00231
Each partner links to its Q-omics profile. Showing the 6 strongest of 6 associations by consensus.

ARMH2 by RFTN2 expression — SOFT_TISSUE

Box plot of ARMH2 in RFTN2-low vs RFTN2-high samples in SOFT_TISSUE.

Explore this box plot interactively →

Exploration