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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking COMT and autistic disorder 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
  • 6254 RGD objects have been annotated to autistic disorder  (DOID:12849)
  • 115 papers in RGD have been used to annotate COMT
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:16917939


  • An association has been curated linking COMT and autistic disorder 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:14351880 (Homo sapiens)
  • 6254 RGD objects have been annotated to autistic disorder  (DOID:12849)
  • 115 papers in RGD have been used to annotate COMT
  • Curation Notes: ClinVar Annotator: match by term: Autistic disorder of childhood onset
  • Original References(s): PMID:21681106 PMID:30208311


  • An association has been curated linking COMT and autistic disorder 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:14351885 (Homo sapiens)
  • 6254 RGD objects have been annotated to autistic disorder  (DOID:12849)
  • 115 papers in RGD have been used to annotate COMT
  • Curation Notes: ClinVar Annotator: match by term: Autistic disorder of childhood onset
  • Original References(s): PMID:21681106 PMID:30208311


  • An association has been curated linking COMT and autistic disorder 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:14351891 (Homo sapiens)
  • 6254 RGD objects have been annotated to autistic disorder  (DOID:12849)
  • 115 papers in RGD have been used to annotate COMT
  • Curation Notes: ClinVar Annotator: match by term: Autistic disorder of childhood onset
  • Original References(s): PMID:21681106 PMID:30208311


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