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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking FGA and congenital afibrinogenemia in Canis lupus familiaris.        

  • 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)
  • 0 papers in RGD have been used to annotate FGA


    • An association has been curated linking FGA and congenital afibrinogenemia in Canis lupus familiaris.        

  • 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)
  • 0 papers in RGD have been used to annotate FGA
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia | ClinVar Annotator: match by term: Congenital afibrinogenemia | ClinVar Annotator: match by term: Factor I deficiency | ClinVar Annotator: match by term: Hypofibrinogenemia
  • Original References(s): PMID:10602365 PMID:10605955 PMID:10887149 PMID:10891444 PMID:10910940 PMID:12050338 PMID:12358944 PMID:12871326 PMID:14615374 PMID:16362348 PMID:16651864 PMID:17576681 PMID:17982313 PMID:19109585 PMID:19420351 PMID:19468208 PMID:22880226 PMID:237956 PMID:23852822 PMID:25320241 PMID:25741868 PMID:25816717 PMID:26006300 PMID:26577257 PMID:26763372 PMID:27164460 PMID:2738154 PMID:27684817 PMID:28101869 PMID:28211264 PMID:28492532 PMID:30332696 PMID:30349899 PMID:30856382 PMID:31064749 PMID:31314131 PMID:31924745 PMID:32166693 PMID:32877852 PMID:3345340 PMID:33668986 PMID:34355501 PMID:3590111 PMID:3618591 PMID:4052020 PMID:6191801 PMID:7298640 PMID:8113408 PMID:8473507 PMID:8636415 PMID:8944230 PMID:9536098


    • An association has been curated linking FGA and congenital afibrinogenemia in Canis lupus familiaris.        

  • 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)
  • 0 papers in RGD have been used to annotate FGA
  • Curation Notes: ClinVar Annotator: match by term: Afibrinogenemia | ClinVar Annotator: match by term: Congenital afibrinogenemia | ClinVar Annotator: match by term: Hypofibrinogenemia
  • Original References(s): PMID:10602365 PMID:10605955 PMID:10887149 PMID:10891444 PMID:10910940 PMID:12050338 PMID:12358944 PMID:12871326 PMID:14615374 PMID:16362348 PMID:16651864 PMID:17576681 PMID:17982313 PMID:19109585 PMID:19420351 PMID:19468208 PMID:22880226 PMID:23852822 PMID:25320241 PMID:25741868 PMID:25816717 PMID:26006300 PMID:26577257 PMID:26763372 PMID:27164460 PMID:2738154 PMID:27684817 PMID:28101869 PMID:28492532 PMID:28912669 PMID:30332696 PMID:30349899 PMID:30856382 PMID:31064749 PMID:31314131 PMID:32166693 PMID:32660897 PMID:32877852 PMID:3345340 PMID:33668986 PMID:34275736 PMID:34355501 PMID:3590111 PMID:3618591 PMID:4052020 PMID:6191801 PMID:7298640 PMID:8113408 PMID:8473507 PMID:8636415 PMID:8944230 PMID:9536098


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