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GENE - TERM ANNOTATION REPORT

22 Annotations Found.

An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: DEAFNESS, AUTOSOMAL DOMINANT 17
  • Original References(s): PMID:11023810 PMID:17146397 PMID:24890873 PMID:25505834 PMID:9390828


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17
  • Original References(s): PMID:24033266 PMID:25741868


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17
  • Original References(s): PMID:24033266


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal dominant 17
  • Original References(s): PMID:11752022 PMID:12533692 PMID:16969870 PMID:23409987 PMID:24186861 PMID:25741868 PMID:26226608


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17
  • Original References(s): PMID:18059020 PMID:24033266


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17
  • Original References(s): PMID:11752022 PMID:18676005 PMID:22123909 PMID:22477015 PMID:22995991 PMID:24033266 PMID:24643058 PMID:25741868 PMID:26467025 PMID:28059092 PMID:29090586 PMID:30720677


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17
  • Original References(s): PMID:23349334 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17
  • Original References(s): PMID:25741868


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17
  • Original References(s): PMID:19557653 PMID:23144074 PMID:24033266 PMID:26346198 PMID:26969326 PMID:27068579 PMID:28492532


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17
  • Original References(s): PMID:28492532


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal dominant 17
  • Original References(s): PMID:25741868 PMID:31064749


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17
  • Original References(s): PMID:24033266 PMID:25752595


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17
  • Original References(s): PMID:11590545 PMID:20588287 PMID:23804846 PMID:24033266 PMID:24643058 PMID:25077172 PMID:25949529


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17
  • Original References(s): PMID:24033266 PMID:24130771 PMID:25077172 PMID:26467025 PMID:28492532 PMID:30720677


  • An association has been curated linking Myh9 and autosomal dominant nonsyndromic deafness 17 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 MYH9 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 17  (DOID:0110548)
  • 50 papers in RGD have been used to annotate Myh9
  • Curation Notes: ClinVar Annotator: match by term: Autosomal dominant nonsyndromic deafness 17
  • Original References(s): PMID:23144074


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