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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking AR and androgen insensitivity syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from Jakubiczka S, etal., Hum Genet. 1992 Nov;90(3):311-2.
  • 3 additional annotations were made from Jakubiczka S, etal., Hum Genet. 1992 Nov;90(3):311-2.
  • 6 RGD objects have been annotated to androgen insensitivity syndrome  (DOID:4674)
  • 64 papers in RGD have been used to annotate AR
  • Curation Notes: DNA:missense mutation:exon:p.M749V (human)


    • An association has been curated linking Ar and androgen insensitivity syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Jakubiczka S, etal., Hum Genet. 1992 Nov;90(3):311-2.
  • The annotation has been inferred from sequence orthology with AR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 additional annotations were made from Jakubiczka S, etal., Hum Genet. 1992 Nov;90(3):311-2.
  • 6 RGD objects have been annotated to androgen insensitivity syndrome  (DOID:4674)
  • 100 papers in RGD have been used to annotate Ar
  • Curation Notes: DNA:missense mutation:exon:p.M749V (human)


    • An association has been curated linking Ar and androgen insensitivity syndrome in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Jakubiczka S, etal., Hum Genet. 1992 Nov;90(3):311-2.
  • The annotation has been inferred from sequence orthology with AR (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 additional annotations were made from Jakubiczka S, etal., Hum Genet. 1992 Nov;90(3):311-2.
  • 6 RGD objects have been annotated to androgen insensitivity syndrome  (DOID:4674)
  • 65 papers in RGD have been used to annotate Ar
  • Curation Notes: DNA:missense mutation:exon:p.M749V (human)


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