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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking Stt3b and congenital disorder of glycosylation Ix 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 STT3B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital disorder of glycosylation Ix  (DOID:0080573)
  • 5 papers in RGD have been used to annotate Stt3b


  • An association has been curated linking Stt3b and congenital disorder of glycosylation Ix 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 STT3B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital disorder of glycosylation Ix  (DOID:0080573)
  • 5 papers in RGD have been used to annotate Stt3b
  • Curation Notes: ClinVar Annotator: match by OMIM:615597
  • Original References(s): PMID:23842455


  • An association has been curated linking Stt3b and congenital disorder of glycosylation Ix 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 STT3B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital disorder of glycosylation Ix  (DOID:0080573)
  • 5 papers in RGD have been used to annotate Stt3b
  • Curation Notes: ClinVar Annotator: match by term: Congenital disorder of glycosylation type 1x
  • Original References(s): PMID:28492532


  • An association has been curated linking Stt3b and congenital disorder of glycosylation Ix 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 STT3B (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital disorder of glycosylation Ix  (DOID:0080573)
  • 5 papers in RGD have been used to annotate Stt3b
  • Curation Notes: ClinVar Annotator: match by term: Congenital disorder of glycosylation type 1x
  • Original References(s): PMID:25741868


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