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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking Fga and congenital afibrinogenemia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with FGA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 57 papers in RGD have been used to annotate Fga


  • An association has been curated linking Fga and congenital afibrinogenemia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Neerman-Arbez M, etal., Eur J Hum Genet. 1999 Dec;7(8):897-902.
  • The annotation has been inferred from sequence orthology with FGA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 additional annotations were made from Neerman-Arbez M, etal., Eur J Hum Genet. 1999 Dec;7(8):897-902.
  • 5 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 57 papers in RGD have been used to annotate Fga
  • Curation Notes: DNA:deletion:cds: (human)


  • An association has been curated linking Fga and congenital afibrinogenemia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Wu S, etal., Blood Coagul Fibrinolysis. 2005 Apr;16(3):221-6.
  • The annotation has been inferred from sequence orthology with FGA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Wu S, etal., Blood Coagul Fibrinolysis. 2005 Apr;16(3):221-6.
  • 5 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 57 papers in RGD have been used to annotate Fga


  • An association has been curated linking Fga and congenital afibrinogenemia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with FGA (Homo sapiens) [(EXP) inferred from experiment]
  • 5 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 57 papers in RGD have been used to annotate Fga
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:1391954 PMID:10602365 PMID:10891444 PMID:12358944


  • An association has been curated linking Fga and congenital afibrinogenemia in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with FGA (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 5 RGD objects have been annotated to congenital afibrinogenemia  (DOID:2236)
  • 57 papers in RGD have been used to annotate Fga
  • Curation Notes: ClinVar Annotator: match by term: Congenital afibrinogenemia | ClinVar Annotator: match by term: Hypofibrinogenemia
  • Original References(s): PMID:10602365 PMID:10887149 PMID:10891444 PMID:10910940 PMID:12358944 PMID:12871326 PMID:14615374 PMID:16362348 PMID:19420351 PMID:22880226 PMID:237956 PMID:25741868 PMID:25816717 PMID:26763372 PMID:27164460 PMID:2738154 PMID:27684817 PMID:28101869 PMID:28211264 PMID:28492532 PMID:30332696 PMID:31064749 PMID:31924745 PMID:3345340 PMID:34355501 PMID:3590111 PMID:3618591 PMID:4052020 PMID:6191801 PMID:7298640


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