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GENE - TERM ANNOTATION REPORT

11 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)
  • 56 papers in RGD have been used to annotate Fga

  • This annotation was curated on 2019-11-27 19:57:10.0 by RGD . For more information contact us

    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)
  • 56 papers in RGD have been used to annotate Fga
  • Curation Notes: ClinVar Annotator: match by OMIM:202400
  • Original References(s): PMID:12358944

  • This annotation was curated on 2019-11-12 07:31:33.0 by RGD . For more information contact us

    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)
  • 56 papers in RGD have been used to annotate Fga
  • Curation Notes: ClinVar Annotator: match by OMIM:202400
  • Original References(s): PMID:10602365, PMID:10891444

  • This annotation was curated on 2019-11-12 07:31:33.0 by RGD . For more information contact us

    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)
  • 56 papers in RGD have been used to annotate Fga
  • Curation Notes: DNA:deletion:cds: (human)

  • This annotation was curated on 2018-05-12 09:00:42.0 by RGD . For more information contact us

    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)
  • 56 papers in RGD have been used to annotate Fga

  • This annotation was curated on 2018-05-12 09:00:51.0 by RGD . For more information contact us

    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)
  • 56 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

  • This annotation was curated on 2019-11-26 04:43:27.0 by RGD . For more information contact us

    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)
  • 56 papers in RGD have been used to annotate Fga
  • Curation Notes: ClinVar Annotator: match by OMIM:202400

  • This annotation was curated on 2019-11-12 07:33:13.0 by RGD . For more information contact us

    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)
  • 56 papers in RGD have been used to annotate Fga
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:25741868

  • This annotation was curated on 2019-11-12 07:31:26.0 by RGD . For more information contact us

    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)
  • 56 papers in RGD have been used to annotate Fga
  • Curation Notes: ClinVar Annotator: match by term: Hypofibrinogenemia
  • Original References(s): PMID:25741868, PMID:2738154, PMID:3345340, PMID:3590111, PMID:3618591, PMID:4052020, PMID:6191801, PMID:7298640

  • This annotation was curated on 2019-11-12 07:29:03.0 by RGD . For more information contact us

    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)
  • 56 papers in RGD have been used to annotate Fga
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:10891444, PMID:14615374, PMID:25741868

  • This annotation was curated on 2019-11-12 07:31:33.0 by RGD . For more information contact us

    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)
  • 56 papers in RGD have been used to annotate Fga
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia, congenital
  • Original References(s): PMID:10318664, PMID:10910940, PMID:16362348, PMID:25741868

  • This annotation was curated on 2019-11-12 07:31:33.0 by RGD . For more information contact us

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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.