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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking Mgat2 and congenital disorder of glycosylation type IIa 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 MGAT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to congenital disorder of glycosylation type IIa  (DOID:0070253)
  • 15 papers in CRRD have been used to annotate Mgat2


  • An association has been curated linking Mgat2 and congenital disorder of glycosylation type IIa 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 MGAT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to congenital disorder of glycosylation type IIa  (DOID:0070253)
  • 15 papers in CRRD have been used to annotate Mgat2
  • Curation Notes: ClinVar Annotator: match by OMIM:212066
  • Original References(s): PMID:11228641


  • An association has been curated linking Mgat2 and congenital disorder of glycosylation type IIa 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 MGAT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to congenital disorder of glycosylation type IIa  (DOID:0070253)
  • 15 papers in CRRD have been used to annotate Mgat2
  • Curation Notes: ClinVar Annotator: match by OMIM:212066
  • Original References(s): PMID:8808595


  • An association has been curated linking Mgat2 and congenital disorder of glycosylation type IIa 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 MGAT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to congenital disorder of glycosylation type IIa  (DOID:0070253)
  • 15 papers in CRRD have been used to annotate Mgat2
  • Curation Notes: ClinVar Annotator: match by OMIM:212066
  • Original References(s): PMID:20684000, PMID:22105986, PMID:25558065


  • An association has been curated linking Mgat2 and congenital disorder of glycosylation type IIa 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 MGAT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to congenital disorder of glycosylation type IIa  (DOID:0070253)
  • 15 papers in CRRD have been used to annotate Mgat2
  • Curation Notes: ClinVar Annotator: match by term: Carbohydrate-deficient glycoprotein syndrome type II
  • Original References(s): PMID:25741868


  • An association has been curated linking Mgat2 and congenital disorder of glycosylation type IIa 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 MGAT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to congenital disorder of glycosylation type IIa  (DOID:0070253)
  • 15 papers in CRRD have been used to annotate Mgat2
  • Curation Notes: ClinVar Annotator: match by term: Carbohydrate-deficient glycoprotein syndrome type II
  • Original References(s): PMID:28492532


  • An association has been curated linking Mgat2 and congenital disorder of glycosylation type IIa 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 MGAT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to congenital disorder of glycosylation type IIa  (DOID:0070253)
  • 15 papers in CRRD have been used to annotate Mgat2
  • Curation Notes: ClinVar Annotator: match by term: Carbohydrate-deficient glycoprotein syndrome type II


  • An association has been curated linking Mgat2 and congenital disorder of glycosylation type IIa 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 MGAT2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 CRRD objects have been annotated to congenital disorder of glycosylation type IIa  (DOID:0070253)
  • 15 papers in CRRD have been used to annotate Mgat2
  • Curation Notes: ClinVar Annotator: match by term: Congenital disorder of glycosylation, type IIa
  • Original References(s): PMID:23806237, PMID:25741868, PMID:28492532


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.