NFATC2IP

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

Across TCGA patient cohorts, NFATC2IP mutation is significantly associated with the RNA expression of many other genes, with 350 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible NFATC2IP-associated genes across cancer lineages are KRTAP9-2, RPL23AP45, and MIR6515. Each is linked with NFATC2IP in more than 1 cancer types. Because this analysis shows association rather than direction, both NFATC2IP-to-partner and partner-to-NFATC2IP results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, KRTAP9-2 grouped by NFATC2IP-low versus NFATC2IP-high in HNSC.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (NFATC2IP→partner) and Y-score (partner→NFATC2IP) 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
HNSCKRTAP9-2 →+0.039+5.401<.001.00132
SKCMRPL23AP45 →+0.098+5.097<.001.00832
BRCAMIR6515 →+0.717+8.055<.001.00731
UCECTEX30 →+0.817+3.459.001.00531
UCECNCAPD3 →+0.812+3.470.001.00331
UCECWHAMM →+0.614+3.386<.001.00431
Each partner links to its Q-omics profile. Showing the 6 strongest of 350 associations by consensus.

KRTAP9-2 by NFATC2IP expression — HNSC

Box plot of KRTAP9-2 in NFATC2IP-low vs NFATC2IP-high samples in HNSC.

Explore this box plot interactively →

Exploration