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GENE - TERM ANNOTATION REPORT

10 Annotations Found.

An association has been curated linking Ampd1 and MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY 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 AMPD1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY  (DOID:9008558)
  • 17 papers in RGD have been used to annotate Ampd1


  • An association has been curated linking Ampd1 and MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY 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 AMPD1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY  (DOID:9008558)
  • 17 papers in RGD have been used to annotate Ampd1
  • Curation Notes: ClinVar Annotator: match by term: Muscle AMP deaminase deficiency


  • An association has been curated linking Ampd1 and MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY 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 AMPD1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY  (DOID:9008558)
  • 17 papers in RGD have been used to annotate Ampd1
  • Curation Notes: ClinVar Annotator: match by term: Muscle AMP deaminase deficiency
  • Original References(s): PMID:25741868


  • An association has been curated linking Ampd1 and MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY 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 AMPD1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY  (DOID:9008558)
  • 17 papers in RGD have been used to annotate Ampd1
  • Curation Notes: ClinVar Annotator: match by term: Muscle AMP deaminase deficiency
  • Original References(s): PMID:28492532


  • An association has been curated linking Ampd1 and MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY 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 AMPD1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY  (DOID:9008558)
  • 17 papers in RGD have been used to annotate Ampd1
  • Curation Notes: ClinVar Annotator: match by term: Muscle AMP deaminase deficiency
  • Original References(s): PMID:10996775 PMID:11102975 PMID:28492532


  • An association has been curated linking Ampd1 and MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY 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 AMPD1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY  (DOID:9008558)
  • 17 papers in RGD have been used to annotate Ampd1
  • Curation Notes: ClinVar Annotator: match by term: Muscle AMP deaminase deficiency
  • Original References(s): PMID:25155876 PMID:28492532


  • An association has been curated linking Ampd1 and MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY 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 AMPD1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY  (DOID:9008558)
  • 17 papers in RGD have been used to annotate Ampd1
  • Curation Notes: ClinVar Annotator: match by term: Muscle AMP deaminase deficiency
  • Original References(s): PMID:15173240 PMID:25741868 PMID:28492532


  • An association has been curated linking Ampd1 and MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY 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 AMPD1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY  (DOID:9008558)
  • 17 papers in RGD have been used to annotate Ampd1
  • Curation Notes: ClinVar Annotator: match by term: Muscle AMP deaminase deficiency
  • Original References(s): PMID:10996775 PMID:11102975 PMID:25741868


  • An association has been curated linking Ampd1 and MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY 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 AMPD1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY  (DOID:9008558)
  • 17 papers in RGD have been used to annotate Ampd1
  • Curation Notes: ClinVar Annotator: match by term: Muscle AMP deaminase deficiency
  • Original References(s): PMID:1631143 PMID:21343608 PMID:25741868 PMID:28492532 PMID:8335021


  • An association has been curated linking Ampd1 and MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY 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 AMPD1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY  (DOID:9008558)
  • 17 papers in RGD have been used to annotate Ampd1
  • Curation Notes: ClinVar Annotator: match by term: Muscle AMP deaminase deficiency
  • Original References(s): PMID:12117480 PMID:25741868 PMID:27296017 PMID:28492532


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