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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Cog1 and congenital disorder of glycosylation type IIg 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 COG1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation type IIg  (DOID:0070259)
  • 5 papers in RGD have been used to annotate Cog1


  • An association has been curated linking Cog1 and congenital disorder of glycosylation type IIg 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 COG1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to congenital disorder of glycosylation type IIg  (DOID:0070259)
  • 5 papers in RGD have been used to annotate Cog1
  • Curation Notes: ClinVar Annotator: match by term: CDGII/COG1 CEREBROCOSTOMANDIBULAR-LIKE SYNDROME | ClinVar Annotator: match by term: Congenital disorder of glycosylation type 2G
  • Original References(s): PMID:16537452 PMID:17576681 PMID:19008299 PMID:23757202 PMID:23806237 PMID:25741868 PMID:27112773 PMID:28492532 PMID:29127259 PMID:9536098


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