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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking Hoxb1 and Hereditary Congenital Facial Paresis 3 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 HOXB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Hereditary Congenital Facial Paresis 3  (DOID:9008662)
  • 6 papers in RGD have been used to annotate Hoxb1


  • An association has been curated linking Hoxb1 and Hereditary Congenital Facial Paresis 3 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 HOXB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Hereditary Congenital Facial Paresis 3  (DOID:9008662)
  • 6 papers in RGD have been used to annotate Hoxb1
  • Curation Notes: ClinVar Annotator: match by OMIM:614744
  • Original References(s): PMID:22770981


  • An association has been curated linking Hoxb1 and Hereditary Congenital Facial Paresis 3 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 HOXB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Hereditary Congenital Facial Paresis 3  (DOID:9008662)
  • 6 papers in RGD have been used to annotate Hoxb1
  • Curation Notes: ClinVar Annotator: match by term: Hereditary congenital facial paresis 3
  • Original References(s): PMID:26007620


  • An association has been curated linking Hoxb1 and Hereditary Congenital Facial Paresis 3 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 HOXB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Hereditary Congenital Facial Paresis 3  (DOID:9008662)
  • 6 papers in RGD have been used to annotate Hoxb1
  • Curation Notes: ClinVar Annotator: match by term: Hereditary congenital facial paresis 3
  • Original References(s): PMID:27144914


  • An association has been curated linking Hoxb1 and Hereditary Congenital Facial Paresis 3 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 HOXB1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Hereditary Congenital Facial Paresis 3  (DOID:9008662)
  • 6 papers in RGD have been used to annotate Hoxb1
  • Curation Notes: ClinVar Annotator: match by term: Hereditary congenital facial paresis 3
  • Original References(s): PMID:25741868


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