Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources

GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking XRCC5 and double-strand break repair via nonhomologous end joining in Homo sapiens.        

  • The association was inferred from electronic annotation (IEA)
    		•  
  • The annotation was made from RGD pipelines: automated import of non-rat, non-mouse GO annotations
  • The annotation has been inferred from electronic annotation with PANTHER:PTHR12604:SF4
  • 76 RGD objects have been annotated to double-strand break repair via nonhomologous end joining  (GO:0006303)
  • 8 papers in RGD have been used to annotate XRCC5
  • Qualifier: involved_in
  • Original References(s): GO_REF:0000118


    • An association has been curated linking XRCC5 and double-strand break repair via nonhomologous end joining in Homo sapiens.        

  • The association was inferred from electronic annotation (IEA)
    		•  
  • The annotation was made from RGD pipelines: automated import of non-rat, non-mouse GO annotations
  • The annotation has been inferred from electronic annotation with InterPro:IPR005160 & InterPro:IPR006164 & InterPro:IPR024193
  • 76 RGD objects have been annotated to double-strand break repair via nonhomologous end joining  (GO:0006303)
  • 8 papers in RGD have been used to annotate XRCC5
  • Qualifier: involved_in
  • Original References(s): GO_REF:0000002


    • An association has been curated linking XRCC5 and double-strand break repair via nonhomologous end joining in Homo sapiens.        

  • The association was inferred from direct assay (IDA)
    		•  
  • The annotation was made from RGD pipelines: automated import of non-rat, non-mouse GO annotations
  • 76 RGD objects have been annotated to double-strand break repair via nonhomologous end joining  (GO:0006303)
  • 8 papers in RGD have been used to annotate XRCC5
  • Qualifier: involved_in
  • Curation Notes: (PMID:26359349)
  • Original References(s): PMID:26359349


    • An association has been curated linking XRCC5 and double-strand break repair via nonhomologous end joining in Homo sapiens.        

  • The association was inferred from mutant phenotype (IMP)
    		•  
  • The annotation was made from RGD pipelines: automated import of non-rat, non-mouse GO annotations
  • 76 RGD objects have been annotated to double-strand break repair via nonhomologous end joining  (GO:0006303)
  • 8 papers in RGD have been used to annotate XRCC5
  • Qualifier: involved_in
  • Curation Notes: (PMID:20383123)
  • Original References(s): PMID:20383123


    • An association has been curated linking XRCC5 and double-strand break repair via nonhomologous end joining in Homo sapiens.        

  • The association was traceable author statement (TAS)
    		•  
  • The annotation was made from RGD pipelines: automated import of non-rat, non-mouse GO annotations
  • 76 RGD objects have been annotated to double-strand break repair via nonhomologous end joining  (GO:0006303)
  • 8 papers in RGD have been used to annotate XRCC5
  • Qualifier: involved_in
  • Curation Notes: (PMID:15824061)
  • Original References(s): PMID:15824061


    • An association has been curated linking XRCC5 and double-strand break repair via nonhomologous end joining in Homo sapiens.        

  • The association was inferred from biological aspect of ancestor (IBA)
    		•  
  • The annotation was made from RGD pipelines: automated import of non-rat, non-mouse GO annotations
  • The annotation has been inferred from biological aspect of ancestor with FB:FBgn0011774 & FB:FBgn0041627 & MGI:95606 & PANTHER:PTN000288287 & PomBase:SPBC543.03c & PomBase:SPCC126.02c & SGD:S000004712 & SGD:S000004897 & TAIR:locus:2023757 & TAIR:locus:2035495 & UniProtKB:P12956 & UniProtKB:P13010 & UniProtKB:Q4WI96 & dictyBase:DDB_G0286303
  • 76 RGD objects have been annotated to double-strand break repair via nonhomologous end joining  (GO:0006303)
  • 8 papers in RGD have been used to annotate XRCC5
  • Qualifier: involved_in
  • Original References(s): GO_REF:0000033


    • An association has been curated linking XRCC5 and double-strand break repair via nonhomologous end joining in Homo sapiens.        

  • The association was non-traceable author statement (NAS)
    		•  
  • The annotation was made from RGD pipelines: automated import of non-rat, non-mouse GO annotations
  • 76 RGD objects have been annotated to double-strand break repair via nonhomologous end joining  (GO:0006303)
  • 8 papers in RGD have been used to annotate XRCC5
  • Qualifier: involved_in
  • Curation Notes: (PMID:10207111), (PMID:9362500)
  • Original References(s): PMID:10207111 PMID:9362500


    • Go Back to source page   Continue to Ontology report