IP6K1

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

Across TCGA cell cohorts, IP6K1 mutation is significantly associated with the drug of many other genes, with 25 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible IP6K1-associated genes across cancer lineages are KRAS (G12C) Inhibitor-12, Dactinomycin, and Ispinesib Mesylate. Each is linked with IP6K1 in more than 1 cancer types. Because this analysis shows association rather than direction, both IP6K1-to-partner and partner-to-IP6K1 results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, KRAS (G12C) Inhibitor-12 grouped by IP6K1-low versus IP6K1-high in LARGE_INTESTINE.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (IP6K1→partner) and Y-score (partner→IP6K1) 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_INTESTINEKRAS (G12C) Inhibitor-12 →+0.550+2.868.019.02231
LARGE_INTESTINEDactinomycin →+0.611+2.649.033.04631
LARGE_INTESTINEIspinesib Mesylate →+0.755+2.874.013.02131
LARGE_INTESTINEGenentech Cpd 10 →+0.735+2.874.009.02131
LARGE_INTESTINEGSK1070916 →+0.606+2.655.043.04431
LARGE_INTESTINESU11274 →+0.499+2.874.010.02131
Each partner links to its Q-omics profile. Showing the 6 strongest of 25 associations by consensus.

KRAS (G12C) Inhibitor-12 by IP6K1 expression — LARGE_INTESTINE

Box plot of KRAS (G12C) Inhibitor-12 in IP6K1-low vs IP6K1-high samples in LARGE_INTESTINE.

Explore this box plot interactively →

Exploration