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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Cog7 and congenital disorder of glycosylation type IIe 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 COG7 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 9 RGD objects have been annotated to congenital disorder of glycosylation type IIe  (DOID:0070257)
  • 7 papers in RGD have been used to annotate Cog7


    • An association has been curated linking Cog7 and congenital disorder of glycosylation type IIe 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 COG7 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 9 RGD objects have been annotated to congenital disorder of glycosylation type IIe  (DOID:0070257)
  • 7 papers in RGD have been used to annotate Cog7
  • Curation Notes: ClinVar Annotator: match by term: COG7 congenital disorder of glycosylation | ClinVar Annotator: match by term: Congenital disorder of glycosylation type 2E
  • Original References(s): PMID:15107842 PMID:16199547 PMID:17356545 PMID:17395513 PMID:17576681 PMID:19577670 PMID:21811164 PMID:25741868 PMID:25741869 PMID:28492532 PMID:30653653 PMID:31785789 PMID:9536098


    • An association has been curated linking Cog7 and congenital disorder of glycosylation type IIe 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 COG7 (Homo sapiens) [(EXP) inferred from experiment]
  • 9 RGD objects have been annotated to congenital disorder of glycosylation type IIe  (DOID:0070257)
  • 7 papers in RGD have been used to annotate Cog7
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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