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GENE - TERM ANNOTATION REPORT

13 Annotations Found.

An association has been curated linking Myh3 and Freeman-Sheldon syndrome 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 MYH3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Freeman-Sheldon syndrome  (DOID:0111604)
  • 11 papers in CRRD have been used to annotate Myh3
  • Curation Notes: ClinVar Annotator: match by OMIM:193700
  • Original References(s): PMID:25741868


  • An association has been curated linking Myh3 and Freeman-Sheldon syndrome 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 MYH3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Freeman-Sheldon syndrome  (DOID:0111604)
  • 11 papers in CRRD have been used to annotate Myh3
  • Curation Notes: ClinVar Annotator: match by OMIM:193700
  • Original References(s): PMID:16642020


  • An association has been curated linking Myh3 and Freeman-Sheldon syndrome 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 MYH3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Freeman-Sheldon syndrome  (DOID:0111604)
  • 11 papers in CRRD have been used to annotate Myh3
  • Curation Notes: ClinVar Annotator: match by term: Freeman-Sheldon syndrome
  • Original References(s): PMID:16642020, PMID:25741868, PMID:30379605


  • An association has been curated linking Myh3 and Freeman-Sheldon syndrome 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 MYH3 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 CRRD objects have been annotated to Freeman-Sheldon syndrome  (DOID:0111604)
  • 11 papers in CRRD have been used to annotate Myh3
  • Curation Notes: CTD Direct Evidence: marker/mechanism


  • An association has been curated linking Myh3 and Freeman-Sheldon syndrome 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 MYH3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Freeman-Sheldon syndrome  (DOID:0111604)
  • 11 papers in CRRD have been used to annotate Myh3
  • Curation Notes: ClinVar Annotator: match by term: Freeman-Sheldon syndrome


  • An association has been curated linking Myh3 and Freeman-Sheldon syndrome 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 MYH3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Freeman-Sheldon syndrome  (DOID:0111604)
  • 11 papers in CRRD have been used to annotate Myh3
  • Curation Notes: ClinVar Annotator: match by term: Freeman-Sheldon syndrome
  • Original References(s): PMID:18414213, PMID:25741868


  • An association has been curated linking Myh3 and Freeman-Sheldon syndrome 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 MYH3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Freeman-Sheldon syndrome  (DOID:0111604)
  • 11 papers in CRRD have been used to annotate Myh3
  • Curation Notes: ClinVar Annotator: match by term: Freeman-Sheldon syndrome
  • Original References(s): PMID:16642020, PMID:18695058, PMID:25741868, PMID:30826400


  • An association has been curated linking Myh3 and Freeman-Sheldon syndrome 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 MYH3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Freeman-Sheldon syndrome  (DOID:0111604)
  • 11 papers in CRRD have been used to annotate Myh3
  • Curation Notes: ClinVar Annotator: match by term: Freeman-Sheldon syndrome
  • Original References(s): PMID:25741868, PMID:28492532


  • An association has been curated linking Myh3 and Freeman-Sheldon syndrome 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 MYH3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Freeman-Sheldon syndrome  (DOID:0111604)
  • 11 papers in CRRD have been used to annotate Myh3
  • Curation Notes: ClinVar Annotator: match by term: Freeman-Sheldon syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking Myh3 and Freeman-Sheldon syndrome 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 MYH3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Freeman-Sheldon syndrome  (DOID:0111604)
  • 11 papers in CRRD have been used to annotate Myh3
  • Curation Notes: ClinVar Annotator: match by term: Freeman-Sheldon syndrome
  • Original References(s): PMID:28492532, PMID:30311386


  • An association has been curated linking Myh3 and Freeman-Sheldon syndrome 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 MYH3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Freeman-Sheldon syndrome  (DOID:0111604)
  • 11 papers in CRRD have been used to annotate Myh3
  • Curation Notes: ClinVar Annotator: match by term: Freeman-Sheldon syndrome
  • Original References(s): PMID:18695058, PMID:25741868


  • An association has been curated linking Myh3 and Freeman-Sheldon syndrome 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 MYH3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Freeman-Sheldon syndrome  (DOID:0111604)
  • 11 papers in CRRD have been used to annotate Myh3
  • Curation Notes: ClinVar Annotator: match by term: Freeman-Sheldon syndrome
  • Original References(s): PMID:19142688


  • An association has been curated linking Myh3 and Freeman-Sheldon syndrome 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 MYH3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Freeman-Sheldon syndrome  (DOID:0111604)
  • 11 papers in CRRD have been used to annotate Myh3
  • Curation Notes: ClinVar Annotator: match by term: Freeman-Sheldon syndrome
  • Original References(s): PMID:29805041


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