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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking ATP7A and Intellectual disability 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:38597596 (Homo sapiens)
  • 3747 RGD objects have been annotated to Intellectual disability  (HP:0001249)
  • 22 papers in RGD have been used to annotate ATP7A
  • Curation Notes: ClinVar Annotator: match by term: Nonprogressive mental retardation
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking ATP7A and Intellectual disability 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:38597595 (Homo sapiens)
  • 3747 RGD objects have been annotated to Intellectual disability  (HP:0001249)
  • 22 papers in RGD have been used to annotate ATP7A
  • Curation Notes: ClinVar Annotator: match by term: Intellectual disability
  • Original References(s): PMID:25741868


  • An association has been curated linking ATP7A and Intellectual disability 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:38494810 (Homo sapiens)
  • 3747 RGD objects have been annotated to Intellectual disability  (HP:0001249)
  • 22 papers in RGD have been used to annotate ATP7A
  • Curation Notes: ClinVar Annotator: match by term: Nonprogressive mental retardation
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking ATP7A and Intellectual disability in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for human HPO-to-gene-to-disease annotations
  • 3747 RGD objects have been annotated to Intellectual disability  (HP:0001249)
  • 22 papers in RGD have been used to annotate ATP7A
  • Original References(s): ORPHA:388


  • An association has been curated linking ATP7A and Intellectual disability in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for human HPO-to-gene-to-disease annotations
  • 3747 RGD objects have been annotated to Intellectual disability  (HP:0001249)
  • 22 papers in RGD have been used to annotate ATP7A
  • Original References(s): ORPHA:565


  • An association has been curated linking ATP7A and Intellectual disability in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for human HPO-to-gene-to-disease annotations
  • 3747 RGD objects have been annotated to Intellectual disability  (HP:0001249)
  • 22 papers in RGD have been used to annotate ATP7A
  • Original References(s): ORPHA:198


  • An association has been curated linking ATP7A and Intellectual disability in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for human HPO-to-gene-to-disease annotations
  • 3747 RGD objects have been annotated to Intellectual disability  (HP:0001249)
  • 22 papers in RGD have been used to annotate ATP7A
  • Original References(s): OMIM:309400


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