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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking AAR2 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:155997283|RGD:156033961|RGD:156067504|RGD:156074823|RGD:156075357|RGD:156190275|RGD:156194343|RGD:156254929|RGD:156394974|RGD:401727276|RGD:401887505 (Homo sapiens) & RGD:155997283|RGD:156033961|RGD:156067504|RGD:156074823|RGD:156075357|RGD:156190275|RGD:156194343|RGD:156254929|RGD:156394974|RGD:401727276|RGD:401887505 (Homo sapiens) & RGD:155997283|RGD:156033961|RGD:156067504|RGD:156074823|RGD:156075357|RGD:156190275|RGD:156194343|RGD:156254929|RGD:156394974|RGD:401727276|RGD:401887505 (Homo sapiens) & RGD:155997283|RGD:156033961|RGD:156067504|RGD:156074823|RGD:156075357|RGD:156190275|RGD:156194343|RGD:156254929|RGD:156394974|RGD:401727276|RGD:401887505 (Homo sapiens) & RGD:155997283|RGD:156033961|RGD:156067504|RGD:156074823|RGD:156075357|RGD:156190275|RGD:156194343|RGD:156254929|RGD:156394974|RGD:401727276|RGD:401887505 (Homo sapiens) & RGD:155997283|RGD:156033961|RGD:156067504|RGD:156074823|RGD:156075357|RGD:156190275|RGD:156194343|RGD:156254929|RGD:156394974|RGD:401727276|RGD:401887505 (Homo sapiens) & RGD:155997283|RGD:156033961|RGD:156067504|RGD:156074823|RGD:156075357|RGD:156190275|RGD:156194343|RGD:156254929|RGD:156394974|RGD:401727276|RGD:401887505 (Homo sapiens) & RGD:155997283|RGD:156033961|RGD:156067504|RGD:156074823|RGD:156075357|RGD:156190275|RGD:156194343|RGD:156254929|RGD:156394974|RGD:401727276|RGD:401887505 (Homo sapiens) & RGD:155997283|RGD:156033961|RGD:156067504|RGD:156074823|RGD:156075357|RGD:156190275|RGD:156194343|RGD:156254929|RGD:156394974|RGD:401727276|RGD:401887505 (Homo sapiens) & RGD:155997283|RGD:156033961|RGD:156067504|RGD:156074823|RGD:156075357|RGD:156190275|RGD:156194343|RGD:156254929|RGD:156394974|RGD:401727276|RGD:401887505 (Homo sapiens) & RGD:155997283|RGD:156033961|RGD:156067504|RGD:156074823|RGD:156075357|RGD:156190275|RGD:156194343|RGD:156254929|RGD:156394974|RGD:401727276|RGD:401887505 (Homo sapiens)
  • 33189 RGD objects have been annotated to genetic disease  (DOID:630)
  • 2 papers in RGD have been used to annotate AAR2
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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