Double-strand break repair via classical nonhomologous end joining
associated omics data
GO:0097680Ontology (GO BP)GO biological process · ~6 member genes
Q-omics provides the Double-strand break repair via classical nonhomologous end joining (GO:0097680) pathway profile, scoring each patient from the combined activity of its roughly 6 member genes. Pathway activity is associated with patient survival in 22 of 34 cancer types, with the highest sampling consensus in ACC. Among the 18 cancer types available for tumor–normal comparison, the pathway is differentially active in 8, with the highest sampling consensus in HNSC. Additionally, pathway RNA activity shows 36,462 significant cross-omics associations, again with the highest sampling consensus in STAD. Together, these results highlight ACC, HNSC, and STAD as cancer lineages where the pathway shows reproducible signals across outcome, tissue activity, and molecular association analyses.
Every result is evaluated using two consensus scores. Sampling consensus measures how consistently a finding is reproduced within a cancer lineage across different conditions. Lineage consensus measures how broadly the result is shared across cancer types, distinguishing pan-cancer signals from lineage-specific patterns. Pathway-against-pathway and pathway-against-mutation comparisons are not available for ontology entities.
Survival associations
This table summarizes Double-strand break repair via classical nonhomologous end joining survival associations by molecular data type. RNA-level pathway activity shows survival associations in the most cancer types (22). The rightmost column indicates the cancer type with the highest sampling consensus for each layer.
This table ranks reproducible pathway activity–survival associations across cancer types. High Double-strand break repair via classical nonhomologous end joining activity shows favorable associations in ACC, LUSC and ESCA, but unfavorable associations in DLBC, LIHC and KICH. In the ACC Kaplan–Meier curve the low-activity group declines faster, consistent with the favorable association (log-rank p < 0.001). ACC ranks highest by sampling consensus for Double-strand break repair via classical nonhomologous end joining.
This table summarizes Double-strand break repair via classical nonhomologous end joining tumor–normal activity differences by data type. RNA-level activity shows significant tumor–normal differences in 8 cancer types, while mass-spec protein activity shows differences in 1. The strongest signals are in KIRC for RNA and COAD for protein.
This table ranks reproducible tumor–normal activity differences for the pathway. A positive fold-change indicates higher activity in tumor tissue. The pathway shows higher tumor activity across HNSC, KIRP, BLCA and LUAD and lower tumor activity in KIRC and THCA. In the HNSC box plot, tumor samples show higher pathway activity than matched normal samples (log2 FC = +0.037, t-test p < 0.001).
This table shows molecular features associated with Double-strand break repair via classical nonhomologous end joining pathway activity in patient tissues and cancer cell lines. In patient samples, pathway activity is most strongly linked to RNA and protein features, with the largest associated set in STAD. In cancer cell lines, RNA-expression features and functional dependencies dominate, with the largest set in PANCREAS.
