IVNS1ABP

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

Across TCGA patient cohorts, IVNS1ABP mutation is significantly associated with the RNA expression of many other genes, with 4,321 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible IVNS1ABP-associated genes across cancer lineages are RNASEH1P2, MIR4797, and OR5AN1. Each is linked with IVNS1ABP in more than 2 cancer types. Because this analysis shows association rather than direction, both IVNS1ABP-to-partner and partner-to-IVNS1ABP results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, RNASEH1P2 grouped by IVNS1ABP-low versus IVNS1ABP-high in CESC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (IVNS1ABP→partner) and Y-score (partner→IVNS1ABP) 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
CESCRNASEH1P2 →+0.093+3.953.007.00333
READMIR4797 →+0.819+5.054<.001.00133
HNSCOR5AN1 →+0.021+4.468<.001.00633
UCECC9orf85 →+0.302+1.686.001.00132
UCECRNF25 →+0.321+2.857<.001<.00132
UCECPGGT1B →+0.310+1.436.009.00632
Each partner links to its Q-omics profile. Showing the 6 strongest of 4,321 associations by consensus.

RNASEH1P2 by IVNS1ABP expression — CESC

Box plot of RNASEH1P2 in IVNS1ABP-low vs IVNS1ABP-high samples in CESC.

Explore this box plot interactively →

Exploration