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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Mycn and Feingold syndrome in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with MYCN (Homo sapiens) [(EXP) inferred from experiment]
  • 2 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 4 papers in RGD have been used to annotate Mycn
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:19852433 PMID:21532573


    • An association has been curated linking Mycn and Feingold syndrome in Mus musculus.        

  • 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 MYCN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to Feingold syndrome  (DOID:0060464)
  • 4 papers in RGD have been used to annotate Mycn
  • Curation Notes: ClinVar Annotator: match by term: Digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum | ClinVar Annotator: match by term: MICROCEPHALY AND DIGITAL ABNORMALITIES WITH NORMAL INTELLIGENCE | ClinVar Annotator: match by term: MMT syndrome | ClinVar Annotator: match by term: Microcephaly-oculo-digito-esophageal-duodenal syndrome
  • Original References(s): PMID:15821734 PMID:16906565 PMID:18470948 PMID:18671284 PMID:20301770 PMID:21224895 PMID:25741868 PMID:28492532 PMID:30573562 PMID:30655312 PMID:33442900


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