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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Mgp and Keutel Syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Munroe PB, etal., Nat Genet. 1999 Jan;21(1):142-4.
  • The annotation has been inferred from sequence orthology with MGP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Munroe PB, etal., Nat Genet. 1999 Jan;21(1):142-4.
  • 1 RGD objects have been annotated to Keutel Syndrome  (DOID:9002991)
  • 31 papers in RGD have been used to annotate Mgp
  • Curation Notes: DNA:deletion,nonsense mutation, splice-site mutation:exon, intron:c.69delG, IVS1-2A>G, c.113T>A (human)


    • An association has been curated linking Mgp and Keutel Syndrome in Rattus norvegicus.        

  • 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 MGP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Keutel Syndrome  (DOID:9002991)
  • 31 papers in RGD have been used to annotate Mgp


    • An association has been curated linking Mgp and Keutel Syndrome in Rattus norvegicus.        

  • 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 MGP (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to Keutel Syndrome  (DOID:9002991)
  • 31 papers in RGD have been used to annotate Mgp
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:21705322


    • An association has been curated linking Mgp and Keutel Syndrome in Rattus norvegicus.        

  • 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 MGP (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Keutel Syndrome  (DOID:9002991)
  • 31 papers in RGD have been used to annotate Mgp
  • Curation Notes: ClinVar Annotator: match by term: Keutel syndrome | ClinVar Annotator: match by term: MGP-related condition
  • Original References(s): PMID:15810001 PMID:25741868 PMID:28492532 PMID:9916809


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