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GENE - TERM ANNOTATION REPORT

14 Annotations Found.

An association has been curated linking Phf6 and Borjeson-Forssman-Lehmann 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 PHF6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Borjeson-Forssman-Lehmann syndrome  (DOID:0050681)
  • 4 papers in RGD have been used to annotate Phf6
  • Curation Notes: ClinVar Annotator: match by OMIM:301900


  • An association has been curated linking Phf6 and Borjeson-Forssman-Lehmann 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 PHF6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Borjeson-Forssman-Lehmann syndrome  (DOID:0050681)
  • 4 papers in RGD have been used to annotate Phf6
  • Curation Notes: ClinVar Annotator: match by OMIM:301900
  • Original References(s): PMID:23906836


  • An association has been curated linking Phf6 and Borjeson-Forssman-Lehmann syndrome 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 PHF6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Borjeson-Forssman-Lehmann syndrome  (DOID:0050681)
  • 4 papers in RGD have been used to annotate Phf6


  • An association has been curated linking Phf6 and Borjeson-Forssman-Lehmann 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 PHF6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Borjeson-Forssman-Lehmann syndrome  (DOID:0050681)
  • 4 papers in RGD have been used to annotate Phf6
  • Curation Notes: ClinVar Annotator: match by OMIM:301900
  • Original References(s): PMID:12415272


  • An association has been curated linking Phf6 and Borjeson-Forssman-Lehmann 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 PHF6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Borjeson-Forssman-Lehmann syndrome  (DOID:0050681)
  • 4 papers in RGD have been used to annotate Phf6
  • Curation Notes: ClinVar Annotator: match by OMIM:301900
  • Original References(s): PMID:12415272 PMID:15466013


  • An association has been curated linking Phf6 and Borjeson-Forssman-Lehmann 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 PHF6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Borjeson-Forssman-Lehmann syndrome  (DOID:0050681)
  • 4 papers in RGD have been used to annotate Phf6
  • Curation Notes: ClinVar Annotator: match by null
  • Original References(s): PMID:15994862


  • An association has been curated linking Phf6 and Borjeson-Forssman-Lehmann 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 PHF6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Borjeson-Forssman-Lehmann syndrome  (DOID:0050681)
  • 4 papers in RGD have been used to annotate Phf6
  • Curation Notes: ClinVar Annotator: match by null
  • Original References(s): PMID:15466013


  • An association has been curated linking Phf6 and Borjeson-Forssman-Lehmann 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 PHF6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Borjeson-Forssman-Lehmann syndrome  (DOID:0050681)
  • 4 papers in RGD have been used to annotate Phf6
  • Curation Notes: ClinVar Annotator: match by OMIM:301900
  • Original References(s): PMID:25741868


  • An association has been curated linking Phf6 and Borjeson-Forssman-Lehmann 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 PHF6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Borjeson-Forssman-Lehmann syndrome  (DOID:0050681)
  • 4 papers in RGD have been used to annotate Phf6
  • Curation Notes: ClinVar Annotator: match by term: Borjeson-Forssman-Lehmann syndrome
  • Original References(s): PMID:25741868 PMID:27633282


  • An association has been curated linking Phf6 and Borjeson-Forssman-Lehmann 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 PHF6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Borjeson-Forssman-Lehmann syndrome  (DOID:0050681)
  • 4 papers in RGD have been used to annotate Phf6
  • Curation Notes: ClinVar Annotator: match by term: Borjeson-Forssman-Lehmann syndrome
  • Original References(s): PMID:18414213 PMID:28492532


  • An association has been curated linking Phf6 and Borjeson-Forssman-Lehmann 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 PHF6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Borjeson-Forssman-Lehmann syndrome  (DOID:0050681)
  • 4 papers in RGD have been used to annotate Phf6
  • Curation Notes: ClinVar Annotator: match by term: Borjeson-Forssman-Lehmann syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking Phf6 and Borjeson-Forssman-Lehmann 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 PHF6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Borjeson-Forssman-Lehmann syndrome  (DOID:0050681)
  • 4 papers in RGD have been used to annotate Phf6
  • Curation Notes: ClinVar Annotator: match by term: Borjeson-Forssman-Lehmann syndrome
  • Original References(s): PMID:24728327 PMID:28492532


  • An association has been curated linking Phf6 and Borjeson-Forssman-Lehmann 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 PHF6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Borjeson-Forssman-Lehmann syndrome  (DOID:0050681)
  • 4 papers in RGD have been used to annotate Phf6
  • Curation Notes: ClinVar Annotator: match by term: Borjeson-Forssman-Lehmann syndrome
  • Original References(s): PMID:12415272 PMID:13871358 PMID:15241480 PMID:25741868


  • An association has been curated linking Phf6 and Borjeson-Forssman-Lehmann 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 PHF6 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Borjeson-Forssman-Lehmann syndrome  (DOID:0050681)
  • 4 papers in RGD have been used to annotate Phf6
  • Curation Notes: ClinVar Annotator: match by term: Borjeson-Forssman-Lehmann syndrome
  • Original References(s): PMID:12415272 PMID:15994862 PMID:25741869 PMID:28492532


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