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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking FGG and Congenital Hypodysfibrinogenemia in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Brennan SO, etal., Hepatology. 2002 Sep;36(3):652-8.
  • 2 additional annotations were made from Brennan SO, etal., Hepatology. 2002 Sep;36(3):652-8.
  • 3 RGD objects have been annotated to Congenital Hypodysfibrinogenemia  (DOID:9004929)
  • 35 papers in RGD have been used to annotate FGG
  • Curation Notes: DNA:missense mutation:exon:p.R375W (human)


  • An association has been curated linking Fgg and Congenital Hypodysfibrinogenemia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Brennan SO, etal., Hepatology. 2002 Sep;36(3):652-8.
  • The annotation has been inferred from sequence orthology with FGG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Brennan SO, etal., Hepatology. 2002 Sep;36(3):652-8.
  • 3 RGD objects have been annotated to Congenital Hypodysfibrinogenemia  (DOID:9004929)
  • 49 papers in RGD have been used to annotate Fgg
  • Curation Notes: DNA:missense mutation:exon:p.R375W (human)


  • An association has been curated linking Fgg and Congenital Hypodysfibrinogenemia in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Brennan SO, etal., Hepatology. 2002 Sep;36(3):652-8.
  • The annotation has been inferred from sequence orthology with FGG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Brennan SO, etal., Hepatology. 2002 Sep;36(3):652-8.
  • 3 RGD objects have been annotated to Congenital Hypodysfibrinogenemia  (DOID:9004929)
  • 43 papers in RGD have been used to annotate Fgg
  • Curation Notes: DNA:missense mutation:exon:p.R375W (human)


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