Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking Hars1 and Charcot-Marie-Tooth disease, axonal type 2W 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 HARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Charcot-Marie-Tooth disease, axonal type 2W  (DOID:0110162)
  • 8 papers in CRRD have been used to annotate Hars1
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, axonal, type 2w
  • Original References(s): PMID:26072516


  • An association has been curated linking Hars1 and Charcot-Marie-Tooth disease, axonal type 2W 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 HARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Charcot-Marie-Tooth disease, axonal type 2W  (DOID:0110162)
  • 8 papers in CRRD have been used to annotate Hars1
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, axonal, type 2w


  • An association has been curated linking Hars1 and Charcot-Marie-Tooth disease, axonal type 2W 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 HARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Charcot-Marie-Tooth disease, axonal type 2W  (DOID:0110162)
  • 8 papers in CRRD have been used to annotate Hars1
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, axonal, type 2w
  • Original References(s): PMID:22930593, PMID:25741868, PMID:27353947, PMID:28492532, PMID:29790872


  • An association has been curated linking Hars1 and Charcot-Marie-Tooth disease, axonal type 2W 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 HARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Charcot-Marie-Tooth disease, axonal type 2W  (DOID:0110162)
  • 8 papers in CRRD have been used to annotate Hars1


  • An association has been curated linking Hars1 and Charcot-Marie-Tooth disease, axonal type 2W 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 HARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Charcot-Marie-Tooth disease, axonal type 2W  (DOID:0110162)
  • 8 papers in CRRD have been used to annotate Hars1
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, axonal, type 2w
  • Original References(s): PMID:28492532, PMID:29235198


  • An association has been curated linking Hars1 and Charcot-Marie-Tooth disease, axonal type 2W 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 HARS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Charcot-Marie-Tooth disease, axonal type 2W  (DOID:0110162)
  • 8 papers in CRRD have been used to annotate Hars1
  • Curation Notes: ClinVar Annotator: match by term: Charcot-Marie-Tooth disease, axonal, type 2w
  • Original References(s): PMID:25741868


  • Go Back to source page   Continue to Ontology report



    NHLBI Logo

    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.