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GENE - TERM ANNOTATION REPORT

18 Annotations Found.

An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(EXP) inferred from experiment]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 5
  • Original References(s): PMID:12690580 PMID:8541851


  • An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 5
  • Original References(s): PMID:12690580 PMID:16769947


  • An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 5
  • Original References(s): PMID:12690580 PMID:25168514 PMID:9879677


  • An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 5
  • Original References(s): PMID:28492532


  • An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 5


  • An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 5
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 5
  • Original References(s): PMID:25741868


  • An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 5
  • Original References(s): PMID:19329989 PMID:26467025 PMID:28160950 PMID:28492532


  • An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 5
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 5
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 5
  • Original References(s): PMID:25614874 PMID:26392352 PMID:28492532


  • An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 5
  • Original References(s): PMID:27790088 PMID:28492532


  • An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 5
  • Original References(s): PMID:16014653 PMID:25168514 PMID:28492532 PMID:31985473


  • An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 5
  • Original References(s): PMID:25741868 PMID:26467025 PMID:27582484 PMID:28492532 PMID:28594869


  • An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 5
  • Original References(s): PMID:19329989 PMID:25741868 PMID:28492532


  • An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 5
  • Original References(s): PMID:16534118 PMID:17595294 PMID:25168514 PMID:25476837 PMID:25741868


  • An association has been curated linking Gars and distal hereditary motor neuronopathy type 5 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 GARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to distal hereditary motor neuronopathy type 5  (DOID:0111203)
  • 9 papers in RGD have been used to annotate Gars
  • Curation Notes: ClinVar Annotator: match by term: Distal hereditary motor neuronopathy type 5
  • Original References(s): PMID:25741868 PMID:29648643


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