Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

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 Meyer M, etal., Blood Coagul Fibrinolysis. 2006 Jan;17(1):63-7.
  • 2 additional annotations were made from Meyer M, etal., Blood Coagul Fibrinolysis. 2006 Jan;17(1):63-7.
  • 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: :p.S313N (7590G>A) (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 Meyer M, etal., Blood Coagul Fibrinolysis. 2006 Jan;17(1):63-7.
  • 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 Meyer M, etal., Blood Coagul Fibrinolysis. 2006 Jan;17(1):63-7.
  • 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: :p.S313N (7590G>A) (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 Meyer M, etal., Blood Coagul Fibrinolysis. 2006 Jan;17(1):63-7.
  • 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 Meyer M, etal., Blood Coagul Fibrinolysis. 2006 Jan;17(1):63-7.
  • 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: :p.S313N (7590G>A) (human)


  • Go Back to source page   Continue to Ontology report