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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

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

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Huang D, etal., Pathology. 2015 Feb;47(2):145-50. doi: 10.1097/PAT.0000000000000213.
  • 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 Huang D, etal., Pathology. 2015 Feb;47(2):145-50. doi: 10.1097/PAT.0000000000000213.
  • 3 RGD objects have been annotated to Congenital Dysfibrinogenemia  (DOID:9003464)
  • 49 papers in RGD have been used to annotate Fgg
  • Curation Notes: DNA:deletion:intron:IVS9+1delG (human)


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

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Liao Z, etal., Clin Chim Acta. 2014 Jan 20;428:106-9.
  • 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 Liao Z, etal., Clin Chim Acta. 2014 Jan 20;428:106-9.
  • 3 RGD objects have been annotated to Congenital Dysfibrinogenemia  (DOID:9003464)
  • 49 papers in RGD have been used to annotate Fgg
  • Curation Notes: DNA:missense mutation:exon:p.N308T (c.1001A>C) (human)


    • An association has been curated linking Fgg and Congenital Dysfibrinogenemia 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 FGG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Congenital Dysfibrinogenemia  (DOID:9003464)
  • 49 papers in RGD have been used to annotate Fgg


    • An association has been curated linking Fgg and Congenital Dysfibrinogenemia 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 FGG (Homo sapiens) [(EXP) inferred from experiment]
  • 3 RGD objects have been annotated to Congenital Dysfibrinogenemia  (DOID:9003464)
  • 49 papers in RGD have been used to annotate Fgg
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking Fgg and Congenital Dysfibrinogenemia 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 FGG (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Congenital Dysfibrinogenemia  (DOID:9003464)
  • 49 papers in RGD have been used to annotate Fgg
  • Curation Notes: ClinVar Annotator: match by term: Dysfibrinogenemia | ClinVar Annotator: match by term: Dysfibrinogenemia, congenital | ClinVar Annotator: match by term: FIBRINOGEN BALTIMORE 3
  • Original References(s): PMID:10688828 PMID:10911375 PMID:11435303 PMID:15795540 PMID:1733971 PMID:17650452 PMID:17849064 PMID:17938819 PMID:19300242 PMID:19923982 PMID:19949684 PMID:20135062 PMID:21228398 PMID:22836217 PMID:23061815 PMID:2328317 PMID:24033266 PMID:2496144 PMID:25039884 PMID:2512677 PMID:25320241 PMID:25741868 PMID:26105150 PMID:2617471 PMID:28211264 PMID:28492532 PMID:29240685 PMID:29351094 PMID:2971042 PMID:2976995 PMID:30349899 PMID:30431218 PMID:30487145 PMID:30632992 PMID:31064749 PMID:31295712 PMID:31352677 PMID:31479941 PMID:3175983 PMID:32852326 PMID:32877852 PMID:3337908 PMID:33443927 PMID:33477601 PMID:34275736 PMID:34355501 PMID:3563970 PMID:35809055 PMID:35853369 PMID:35975558 PMID:37583269 PMID:4002201 PMID:6654188 PMID:6886002 PMID:7635941 PMID:7654933


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