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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Esco2 and Roberts syndrome in Ictidomys tridecemlineatus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with ESCO2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Roberts syndrome  (DOID:5325)
  • 0 papers in RGD have been used to annotate Esco2


    • An association has been curated linking Esco2 and Roberts syndrome in Ictidomys tridecemlineatus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with ESCO2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Roberts syndrome  (DOID:5325)
  • 0 papers in RGD have been used to annotate Esco2
  • Curation Notes: ClinVar Annotator: match by term: ESCO2-related condition | ClinVar Annotator: match by term: Roberts syndrome | ClinVar Annotator: match by term: Roberts-SC phocomelia syndrome
  • Original References(s): PMID:15821733 PMID:16199547 PMID:16380922 PMID:1642282 PMID:16775838 PMID:18411254 PMID:18414213 PMID:19574259 PMID:20101700 PMID:20301332 PMID:24864645 PMID:25741868 PMID:26710928 PMID:28492532 PMID:30508616 PMID:30590172 PMID:31192177 PMID:31976146 PMID:3740099 PMID:495649


    • An association has been curated linking Esco2 and Roberts syndrome in Ictidomys tridecemlineatus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with ESCO2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Roberts syndrome  (DOID:5325)
  • 0 papers in RGD have been used to annotate Esco2
  • Curation Notes: ClinVar Annotator: match by term: ESCO2-related condition | ClinVar Annotator: match by term: Roberts syndrome | ClinVar Annotator: match by term: Roberts-SC phocomelia syndrome
  • Original References(s): PMID:15821733 PMID:16199547 PMID:16380922 PMID:1642282 PMID:16775838 PMID:18411254 PMID:18414213 PMID:19574259 PMID:19738907 PMID:20101700 PMID:20301332 PMID:24864645 PMID:25741868 PMID:26710928 PMID:28492532 PMID:30508616 PMID:30590172 PMID:31192177 PMID:31976146 PMID:32255174 PMID:32977150 PMID:3740099 PMID:495649


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