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GENE - TERM ANNOTATION REPORT

9 Annotations Found.

An association has been curated linking Rars1 and hypomyelinating leukodystrophy 9 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 RARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hypomyelinating leukodystrophy 9  (DOID:0060791)
  • 9 papers in RGD have been used to annotate Rars1


    • An association has been curated linking Rars1 and hypomyelinating leukodystrophy 9 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 RARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hypomyelinating leukodystrophy 9  (DOID:0060791)
  • 9 papers in RGD have been used to annotate Rars1
  • Curation Notes: ClinVar Annotator: match by OMIM:616140
  • Original References(s): PMID:24777941


    • An association has been curated linking Rars1 and hypomyelinating leukodystrophy 9 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 RARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hypomyelinating leukodystrophy 9  (DOID:0060791)
  • 9 papers in RGD have been used to annotate Rars1
  • Curation Notes: ClinVar Annotator: match by term: Leukodystrophy, hypomyelinating, 9
  • Original References(s): PMID:28905880


    • An association has been curated linking Rars1 and hypomyelinating leukodystrophy 9 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 RARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hypomyelinating leukodystrophy 9  (DOID:0060791)
  • 9 papers in RGD have been used to annotate Rars1
  • Curation Notes: ClinVar Annotator: match by term: Leukodystrophy, hypomyelinating, 9
  • Original References(s): PMID:24777941 PMID:25741868


    • An association has been curated linking Rars1 and hypomyelinating leukodystrophy 9 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 RARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hypomyelinating leukodystrophy 9  (DOID:0060791)
  • 9 papers in RGD have been used to annotate Rars1
  • Curation Notes: ClinVar Annotator: match by term: Leukodystrophy, hypomyelinating, 9
  • Original References(s): PMID:24777941 PMID:25741868 PMID:28905880


    • An association has been curated linking Rars1 and hypomyelinating leukodystrophy 9 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 RARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hypomyelinating leukodystrophy 9  (DOID:0060791)
  • 9 papers in RGD have been used to annotate Rars1
  • Curation Notes: ClinVar Annotator: match by term: Leukodystrophy, hypomyelinating, 9
  • Original References(s): PMID:24777941 PMID:27848944 PMID:28492532 PMID:30791064


    • An association has been curated linking Rars1 and hypomyelinating leukodystrophy 9 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 RARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hypomyelinating leukodystrophy 9  (DOID:0060791)
  • 9 papers in RGD have been used to annotate Rars1
  • Curation Notes: ClinVar Annotator: match by term: Leukodystrophy, hypomyelinating, 9
  • Original References(s): PMID:25741868 PMID:28905880


    • An association has been curated linking Rars1 and hypomyelinating leukodystrophy 9 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 RARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hypomyelinating leukodystrophy 9  (DOID:0060791)
  • 9 papers in RGD have been used to annotate Rars1
  • Curation Notes: ClinVar Annotator: match by term: Leukodystrophy, hypomyelinating, 9
  • Original References(s): PMID:25741868


    • An association has been curated linking Rars1 and hypomyelinating leukodystrophy 9 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 RARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to hypomyelinating leukodystrophy 9  (DOID:0060791)
  • 9 papers in RGD have been used to annotate Rars1
  • Curation Notes: ClinVar Annotator: match by term: Leukodystrophy, hypomyelinating, 9


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