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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking APPL1 and genetic disease 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:151709049 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate APPL1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


    • An association has been curated linking APPL1 and genetic disease 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:156021268|RGD:156054846|RGD:156090391|RGD:156131440|RGD:156136261|RGD:156295352|RGD:401733002|RGD:401762413|RGD:401879486|RGD:401895660 (Homo sapiens) & RGD:156021268|RGD:156054846|RGD:156090391|RGD:156131440|RGD:156136261|RGD:156295352|RGD:401733002|RGD:401762413|RGD:401879486|RGD:401895660 (Homo sapiens) & RGD:156021268|RGD:156054846|RGD:156090391|RGD:156131440|RGD:156136261|RGD:156295352|RGD:401733002|RGD:401762413|RGD:401879486|RGD:401895660 (Homo sapiens) & RGD:156021268|RGD:156054846|RGD:156090391|RGD:156131440|RGD:156136261|RGD:156295352|RGD:401733002|RGD:401762413|RGD:401879486|RGD:401895660 (Homo sapiens) & RGD:156021268|RGD:156054846|RGD:156090391|RGD:156131440|RGD:156136261|RGD:156295352|RGD:401733002|RGD:401762413|RGD:401879486|RGD:401895660 (Homo sapiens) & RGD:156021268|RGD:156054846|RGD:156090391|RGD:156131440|RGD:156136261|RGD:156295352|RGD:401733002|RGD:401762413|RGD:401879486|RGD:401895660 (Homo sapiens) & RGD:156021268|RGD:156054846|RGD:156090391|RGD:156131440|RGD:156136261|RGD:156295352|RGD:401733002|RGD:401762413|RGD:401879486|RGD:401895660 (Homo sapiens) & RGD:156021268|RGD:156054846|RGD:156090391|RGD:156131440|RGD:156136261|RGD:156295352|RGD:401733002|RGD:401762413|RGD:401879486|RGD:401895660 (Homo sapiens) & RGD:156021268|RGD:156054846|RGD:156090391|RGD:156131440|RGD:156136261|RGD:156295352|RGD:401733002|RGD:401762413|RGD:401879486|RGD:401895660 (Homo sapiens) & RGD:156021268|RGD:156054846|RGD:156090391|RGD:156131440|RGD:156136261|RGD:156295352|RGD:401733002|RGD:401762413|RGD:401879486|RGD:401895660 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate APPL1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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