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GENE - TERM ANNOTATION REPORT

17 Annotations Found.

An association has been curated linking ARNT2 and Webb-Dattani Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:21068802 (Homo sapiens)
  • 1 RGD objects have been annotated to Webb-Dattani Syndrome  (DOID:9005676)
  • 7 papers in RGD have been used to annotate ARNT2
  • Curation Notes: ClinVar Annotator: match by term: Webb-Dattani syndrome


  • An association has been curated linking ARNT2 and Webb-Dattani Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:21069923 (Homo sapiens)
  • 1 RGD objects have been annotated to Webb-Dattani Syndrome  (DOID:9005676)
  • 7 papers in RGD have been used to annotate ARNT2
  • Curation Notes: ClinVar Annotator: match by term: Webb-Dattani syndrome
  • Original References(s): PMID:24022475


  • An association has been curated linking ARNT2 and Webb-Dattani Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to Webb-Dattani Syndrome  (DOID:9005676)
  • 7 papers in RGD have been used to annotate ARNT2


  • An association has been curated linking ARNT2 and Webb-Dattani Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:150407731 (Homo sapiens)
  • 1 RGD objects have been annotated to Webb-Dattani Syndrome  (DOID:9005676)
  • 7 papers in RGD have been used to annotate ARNT2
  • Curation Notes: ClinVar Annotator: match by term: Webb-Dattani syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking ARNT2 and Webb-Dattani Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:150407728 (Homo sapiens)
  • 1 RGD objects have been annotated to Webb-Dattani Syndrome  (DOID:9005676)
  • 7 papers in RGD have been used to annotate ARNT2
  • Curation Notes: ClinVar Annotator: match by term: Webb-Dattani syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking ARNT2 and Webb-Dattani Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:150407725 (Homo sapiens)
  • 1 RGD objects have been annotated to Webb-Dattani Syndrome  (DOID:9005676)
  • 7 papers in RGD have been used to annotate ARNT2
  • Curation Notes: ClinVar Annotator: match by term: Webb-Dattani syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking ARNT2 and Webb-Dattani Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:150407733 (Homo sapiens)
  • 1 RGD objects have been annotated to Webb-Dattani Syndrome  (DOID:9005676)
  • 7 papers in RGD have been used to annotate ARNT2
  • Curation Notes: ClinVar Annotator: match by term: Webb-Dattani syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking ARNT2 and Webb-Dattani Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:127296330 (Homo sapiens)
  • 1 RGD objects have been annotated to Webb-Dattani Syndrome  (DOID:9005676)
  • 7 papers in RGD have been used to annotate ARNT2
  • Curation Notes: ClinVar Annotator: match by term: Webb-Dattani syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking ARNT2 and Webb-Dattani Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:40815160 (Homo sapiens)
  • 1 RGD objects have been annotated to Webb-Dattani Syndrome  (DOID:9005676)
  • 7 papers in RGD have been used to annotate ARNT2
  • Curation Notes: ClinVar Annotator: match by term: Webb-Dattani syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking ARNT2 and Webb-Dattani Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:126739120 (Homo sapiens)
  • 1 RGD objects have been annotated to Webb-Dattani Syndrome  (DOID:9005676)
  • 7 papers in RGD have been used to annotate ARNT2
  • Curation Notes: ClinVar Annotator: match by term: Webb-Dattani syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking ARNT2 and Webb-Dattani Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:151662425 (Homo sapiens)
  • 1 RGD objects have been annotated to Webb-Dattani Syndrome  (DOID:9005676)
  • 7 papers in RGD have been used to annotate ARNT2
  • Curation Notes: ClinVar Annotator: match by term: Webb-Dattani syndrome


  • An association has been curated linking ARNT2 and Webb-Dattani Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:151662427 (Homo sapiens)
  • 1 RGD objects have been annotated to Webb-Dattani Syndrome  (DOID:9005676)
  • 7 papers in RGD have been used to annotate ARNT2
  • Curation Notes: ClinVar Annotator: match by term: Webb-Dattani syndrome


  • An association has been curated linking ARNT2 and Webb-Dattani Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:21068804 (Homo sapiens)
  • 1 RGD objects have been annotated to Webb-Dattani Syndrome  (DOID:9005676)
  • 7 papers in RGD have been used to annotate ARNT2
  • Curation Notes: ClinVar Annotator: match by term: Webb-Dattani syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking ARNT2 and Webb-Dattani Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:127313208 (Homo sapiens)
  • 1 RGD objects have been annotated to Webb-Dattani Syndrome  (DOID:9005676)
  • 7 papers in RGD have been used to annotate ARNT2
  • Curation Notes: ClinVar Annotator: match by term: Webb-Dattani syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking ARNT2 and Webb-Dattani Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:15176330 (Homo sapiens)
  • 1 RGD objects have been annotated to Webb-Dattani Syndrome  (DOID:9005676)
  • 7 papers in RGD have been used to annotate ARNT2
  • Curation Notes: ClinVar Annotator: match by term: Webb-Dattani syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking ARNT2 and Webb-Dattani Syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:152094177 (Homo sapiens)
  • 1 RGD objects have been annotated to Webb-Dattani Syndrome  (DOID:9005676)
  • 7 papers in RGD have been used to annotate ARNT2
  • Curation Notes: ClinVar Annotator: match by term: Webb-Dattani syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking ARNT2 and Webb-Dattani Syndrome in Homo sapiens.        

  • The association was inferred from experiment (EXP)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 1 RGD objects have been annotated to Webb-Dattani Syndrome  (DOID:9005676)
  • 7 papers in RGD have been used to annotate ARNT2
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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