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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking HCAR2 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:155924755|RGD:155925705|RGD:155977159|RGD:156003631|RGD:156032669|RGD:156067075|RGD:156087455|RGD:156143477|RGD:156274239|RGD:156276736|RGD:156307542|RGD:156339072|RGD:329389379|RGD:401748707|RGD:401773828 (Homo sapiens) & RGD:155924755|RGD:155925705|RGD:155977159|RGD:156003631|RGD:156032669|RGD:156067075|RGD:156087455|RGD:156143477|RGD:156274239|RGD:156276736|RGD:156307542|RGD:156339072|RGD:329389379|RGD:401748707|RGD:401773828 (Homo sapiens) & RGD:155924755|RGD:155925705|RGD:155977159|RGD:156003631|RGD:156032669|RGD:156067075|RGD:156087455|RGD:156143477|RGD:156274239|RGD:156276736|RGD:156307542|RGD:156339072|RGD:329389379|RGD:401748707|RGD:401773828 (Homo sapiens) & RGD:155924755|RGD:155925705|RGD:155977159|RGD:156003631|RGD:156032669|RGD:156067075|RGD:156087455|RGD:156143477|RGD:156274239|RGD:156276736|RGD:156307542|RGD:156339072|RGD:329389379|RGD:401748707|RGD:401773828 (Homo sapiens) & RGD:155924755|RGD:155925705|RGD:155977159|RGD:156003631|RGD:156032669|RGD:156067075|RGD:156087455|RGD:156143477|RGD:156274239|RGD:156276736|RGD:156307542|RGD:156339072|RGD:329389379|RGD:401748707|RGD:401773828 (Homo sapiens) & RGD:155924755|RGD:155925705|RGD:155977159|RGD:156003631|RGD:156032669|RGD:156067075|RGD:156087455|RGD:156143477|RGD:156274239|RGD:156276736|RGD:156307542|RGD:156339072|RGD:329389379|RGD:401748707|RGD:401773828 (Homo sapiens) & RGD:155924755|RGD:155925705|RGD:155977159|RGD:156003631|RGD:156032669|RGD:156067075|RGD:156087455|RGD:156143477|RGD:156274239|RGD:156276736|RGD:156307542|RGD:156339072|RGD:329389379|RGD:401748707|RGD:401773828 (Homo sapiens) & RGD:155924755|RGD:155925705|RGD:155977159|RGD:156003631|RGD:156032669|RGD:156067075|RGD:156087455|RGD:156143477|RGD:156274239|RGD:156276736|RGD:156307542|RGD:156339072|RGD:329389379|RGD:401748707|RGD:401773828 (Homo sapiens) & RGD:155924755|RGD:155925705|RGD:155977159|RGD:156003631|RGD:156032669|RGD:156067075|RGD:156087455|RGD:156143477|RGD:156274239|RGD:156276736|RGD:156307542|RGD:156339072|RGD:329389379|RGD:401748707|RGD:401773828 (Homo sapiens) & RGD:155924755|RGD:155925705|RGD:155977159|RGD:156003631|RGD:156032669|RGD:156067075|RGD:156087455|RGD:156143477|RGD:156274239|RGD:156276736|RGD:156307542|RGD:156339072|RGD:329389379|RGD:401748707|RGD:401773828 (Homo sapiens) & RGD:155924755|RGD:155925705|RGD:155977159|RGD:156003631|RGD:156032669|RGD:156067075|RGD:156087455|RGD:156143477|RGD:156274239|RGD:156276736|RGD:156307542|RGD:156339072|RGD:329389379|RGD:401748707|RGD:401773828 (Homo sapiens) & RGD:155924755|RGD:155925705|RGD:155977159|RGD:156003631|RGD:156032669|RGD:156067075|RGD:156087455|RGD:156143477|RGD:156274239|RGD:156276736|RGD:156307542|RGD:156339072|RGD:329389379|RGD:401748707|RGD:401773828 (Homo sapiens) & RGD:155924755|RGD:155925705|RGD:155977159|RGD:156003631|RGD:156032669|RGD:156067075|RGD:156087455|RGD:156143477|RGD:156274239|RGD:156276736|RGD:156307542|RGD:156339072|RGD:329389379|RGD:401748707|RGD:401773828 (Homo sapiens) & RGD:155924755|RGD:155925705|RGD:155977159|RGD:156003631|RGD:156032669|RGD:156067075|RGD:156087455|RGD:156143477|RGD:156274239|RGD:156276736|RGD:156307542|RGD:156339072|RGD:329389379|RGD:401748707|RGD:401773828 (Homo sapiens) & RGD:155924755|RGD:155925705|RGD:155977159|RGD:156003631|RGD:156032669|RGD:156067075|RGD:156087455|RGD:156143477|RGD:156274239|RGD:156276736|RGD:156307542|RGD:156339072|RGD:329389379|RGD:401748707|RGD:401773828 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 3 papers in RGD have been used to annotate HCAR2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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