CHRFAM7A

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

Across TCGA cell cohorts, CHRFAM7A mutation is significantly associated with the RNA expression of many other genes, with 3 significant associations in total. LARGE_INTESTINE shows the largest number of these associations.

The most reproducible CHRFAM7A-associated genes across cancer lineages are C1QTNF7, ACER1, and CT45A8. Each is linked with CHRFAM7A in more than 1 cancer types. Because this analysis shows association rather than direction, both CHRFAM7A-to-partner and partner-to-CHRFAM7A results are reported.

Each partner links to its own Q-omics profile. The box plot shows the strongest example, C1QTNF7 grouped by CHRFAM7A-low versus CHRFAM7A-high in LARGE_INTESTINE.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (CHRFAM7A→partner) and Y-score (partner→CHRFAM7A) 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_INTESTINEC1QTNF7 →+0.098+4.108<.001.00831
LARGE_INTESTINEACER1 →+0.120+3.823<.001.00631
LARGE_INTESTINECT45A8 →+0.024+3.793.001.00731
Each partner links to its Q-omics profile. Showing the 3 strongest of 3 associations by consensus.

C1QTNF7 by CHRFAM7A expression — LARGE_INTESTINE

Box plot of C1QTNF7 in CHRFAM7A-low vs CHRFAM7A-high samples in LARGE_INTESTINE.

Explore this box plot interactively →

Exploration