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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Fcsk and Congenital Disorder of Glycosylation with Defective Fucosylation 2 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 FCSK (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Congenital Disorder of Glycosylation with Defective Fucosylation 2  (DOID:9001746)
  • 7 papers in RGD have been used to annotate Fcsk


    • An association has been curated linking Fcsk and Congenital Disorder of Glycosylation with Defective Fucosylation 2 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 FCSK (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Congenital Disorder of Glycosylation with Defective Fucosylation 2  (DOID:9001746)
  • 7 papers in RGD have been used to annotate Fcsk
  • Curation Notes: ClinVar Annotator: match by term: Congenital disorder of glycosylation with defective fucosylation 2 | ClinVar Annotator: match by term: FCSK-related condition
  • Original References(s): PMID:16199547 PMID:25741868 PMID:28492532 PMID:30503518


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