HSPA1L

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

Across TCGA cell cohorts, HSPA1L mutation is significantly associated with the drug of many other genes, with 16 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible HSPA1L-associated genes across cancer lineages are NSC-207895, kb NB 142-70, and RU-SKI 43. Each is linked with HSPA1L in more than 1 cancer types. Because this analysis shows association rather than direction, both HSPA1L-to-partner and partner-to-HSPA1L results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (HSPA1L→partner) and Y-score (partner→HSPA1L) 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
LARGE_INTESTINENSC-207895 →+0.637+2.914.001.01231
LARGE_INTESTINEkb NB 142-70 →+0.458+2.874.041.02131
BLOOD_LeukemiaRU-SKI 43 →+0.377+2.845.009.02831
LARGE_INTESTINESabutoclax →+0.501+2.991.011.01821
LARGE_INTESTINEQuizartinib →+0.439+2.874.003.02112
LARGE_INTESTINEAra-G →+0.186+2.944.019.01821
Each partner links to its Q-omics profile. Showing the 6 strongest of 16 associations by consensus.

Exploration