Human Gene Set: GOCC_SITE_OF_DOUBLE_STRAND_BREAK

For the Mouse gene set with the same name, see GOCC_SITE_OF_DOUBLE_STRAND_BREAK

Standard name GOCC_SITE_OF_DOUBLE_STRAND_BREAK
Systematic name M17800
Brief description A region of a chromosome at which a DNA double-strand break has occurred. DNA damage signaling and repair proteins accumulate at the lesion to respond to the damage and repair the DNA to form a continuous DNA helix. [GOC:bf, GOC:mah, GOC:vw, PMID:20096808, PMID:21035408]
Full description or abstract  
Collection C5: Ontology
      GO: Gene Ontology
            GO:CC: GO Cellular Component
Source publication  
Exact source GO:0035861
Related gene sets  
External links http://amigo.geneontology.org/amigo/term/GO:0035861
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Source species Homo sapiens
Contributed by Gene Ontology (Gene Ontology Consortium)
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
Dataset references  
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Version history 2024.1.Hs: Updated to GO Release 2024-04-24.

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