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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Alg3 and congenital disorder of glycosylation Id 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 ALG3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 25 RGD objects have been annotated to congenital disorder of glycosylation Id  (DOID:0080556)
  • 9 papers in RGD have been used to annotate Alg3


    • An association has been curated linking Alg3 and congenital disorder of glycosylation Id 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 ALG3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 25 RGD objects have been annotated to congenital disorder of glycosylation Id  (DOID:0080556)
  • 9 papers in RGD have been used to annotate Alg3
  • Curation Notes: ClinVar Annotator: match by term: CDGS, TYPE IV | ClinVar Annotator: match by term: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id | ClinVar Annotator: match by term: Congenital disorder of glycosylation type 1D
  • Original References(s): PMID:10581255 PMID:11181649 PMID:12357336 PMID:15108280 PMID:15359379 PMID:15840742 PMID:16006436 PMID:16199547 PMID:17551933 PMID:18679822 PMID:19862844 PMID:22642865 PMID:23806237 PMID:25741868 PMID:25741915 PMID:27172925 PMID:28492532 PMID:29667327 PMID:30167849 PMID:31067009 PMID:33187827 PMID:33583022 PMID:34090370 PMID:8552211


    • An association has been curated linking Alg3 and congenital disorder of glycosylation Id 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 ALG3 (Homo sapiens) [(EXP) inferred from experiment]
  • 25 RGD objects have been annotated to congenital disorder of glycosylation Id  (DOID:0080556)
  • 9 papers in RGD have been used to annotate Alg3
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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