KLHL22

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

Across TCGA cell cohorts, KLHL22 mutation is significantly associated with the RNA expression of many other genes, with 18 significant associations in total. BLOOD_Leukemia shows the largest number of these associations.

The most reproducible KLHL22-associated genes across cancer lineages are GP9, CLDN8, and TLX3. Each is linked with KLHL22 in more than 1 cancer types. Because this analysis shows association rather than direction, both KLHL22-to-partner and partner-to-KLHL22 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, GP9 grouped by KLHL22-low versus KLHL22-high in CNS.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (KLHL22→partner) and Y-score (partner→KLHL22) 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
CNSGP9 →+0.025+5.754<.001.00232
BLOOD_LeukemiaCLDN8 →+0.012+4.234<.001.00331
BLOOD_LeukemiaTLX3 →+1.448+3.944.002.00631
BLOOD_LeukemiaKRT6C →+0.026+4.037<.001.00431
BLOOD_LeukemiaPRM3 →+0.054+4.984<.001.00231
BLOOD_LeukemiaDEFB125 →+0.028+4.060<.001.00331
Each partner links to its Q-omics profile. Showing the 6 strongest of 18 associations by consensus.

GP9 by KLHL22 expression — CNS

Box plot of GP9 in KLHL22-low vs KLHL22-high samples in CNS.

Explore this box plot interactively →

Exploration