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

4 Annotations Found.

An association has been curated linking ERCC2 and acute myeloid leukemia in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Automated assignment of GO, PW and RDO ISO annotations across species
  • The annotation has been inferred from sequence orthology with ERCC2 (Homo sapiens)
  • 318 RGD objects have been annotated to acute myeloid leukemia  (DOID:9119)
  • 0 papers in RGD have been used to annotate ERCC2
  • Qualifier: disease_progression
  • Curation Notes: DNA:polymorphism: :p.K751Q (rs13181) (human)
  • Original References(s): PMID:20141440 REF_RGD_ID:11252173


    • An association has been curated linking ERCC2 and acute myeloid leukemia in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Automated assignment of GO, PW and RDO ISO annotations across species
  • The annotation has been inferred from sequence orthology with ERCC2 (Homo sapiens)
  • 318 RGD objects have been annotated to acute myeloid leukemia  (DOID:9119)
  • 0 papers in RGD have been used to annotate ERCC2
  • Qualifier: no_association
  • Curation Notes: DNA:polymorphism: :p.K751Q (rs13181) (human)
  • Original References(s): PMID:23397959 REF_RGD_ID:11252193


    • An association has been curated linking ERCC2 and acute myeloid leukemia in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Automated assignment of GO, PW and RDO ISO annotations across species
  • The annotation has been inferred from sequence orthology with ERCC2 (Homo sapiens)
  • 318 RGD objects have been annotated to acute myeloid leukemia  (DOID:9119)
  • 0 papers in RGD have been used to annotate ERCC2
  • Qualifier: disease_progression
  • Curation Notes: DNA:SNPs, haplotypes: :p.D312N, p.K751Q (human)
  • Original References(s): PMID:21394217 REF_RGD_ID:11252209


    • An association has been curated linking ERCC2 and acute myeloid leukemia in Sus scrofa.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Automated assignment of GO, PW and RDO ISO annotations across species
  • The annotation has been inferred from sequence orthology with ERCC2 (Homo sapiens)
  • 318 RGD objects have been annotated to acute myeloid leukemia  (DOID:9119)
  • 0 papers in RGD have been used to annotate ERCC2
  • Curation Notes: associated with Myeloproliferative Disorders;DNA:polymorphism: :p.K751Q (rs13181) (human)
  • Original References(s): PMID:22496165 REF_RGD_ID:11252198


    • Go Back to source page   Continue to Ontology report