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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking TOGARAM1 and Joubert Syndrome 37 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 Joubert Syndrome 37  (DOID:9007319)
  • 3 papers in RGD have been used to annotate TOGARAM1


    • An association has been curated linking TOGARAM1 and Joubert Syndrome 37 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:34891635 (Homo sapiens)
  • 1 RGD objects have been annotated to Joubert Syndrome 37  (DOID:9007319)
  • 3 papers in RGD have been used to annotate TOGARAM1
  • Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 37
  • Original References(s): PMID:32453716 PMID:32747439


    • An association has been curated linking TOGARAM1 and Joubert Syndrome 37 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:42723039 (Homo sapiens)
  • 1 RGD objects have been annotated to Joubert Syndrome 37  (DOID:9007319)
  • 3 papers in RGD have been used to annotate TOGARAM1
  • Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 37
  • Original References(s): PMID:32747439


    • An association has been curated linking TOGARAM1 and Joubert Syndrome 37 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:40816074|RGD:40816075|RGD:40816076|RGD:40816079|RGD:40886777 (Homo sapiens) & RGD:40816074|RGD:40816075|RGD:40816076|RGD:40816079|RGD:40886777 (Homo sapiens) & RGD:40816074|RGD:40816075|RGD:40816076|RGD:40816079|RGD:40886777 (Homo sapiens) & RGD:40816074|RGD:40816075|RGD:40816076|RGD:40816079|RGD:40886777 (Homo sapiens) & RGD:40816074|RGD:40816075|RGD:40816076|RGD:40816079|RGD:40886777 (Homo sapiens)
  • 1 RGD objects have been annotated to Joubert Syndrome 37  (DOID:9007319)
  • 3 papers in RGD have been used to annotate TOGARAM1
  • Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 37
  • Original References(s): PMID:32453716


    • An association has been curated linking TOGARAM1 and Joubert Syndrome 37 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:155265313|RGD:155266614|RGD:243051098|RGD:401946636 (Homo sapiens) & RGD:155265313|RGD:155266614|RGD:243051098|RGD:401946636 (Homo sapiens) & RGD:155265313|RGD:155266614|RGD:243051098|RGD:401946636 (Homo sapiens) & RGD:155265313|RGD:155266614|RGD:243051098|RGD:401946636 (Homo sapiens)
  • 1 RGD objects have been annotated to Joubert Syndrome 37  (DOID:9007319)
  • 3 papers in RGD have been used to annotate TOGARAM1
  • Curation Notes: ClinVar Annotator: match by term: Joubert syndrome 37
  • Original References(s): PMID:25741868


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