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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Glul and Glutamine Deficiency, Congenital in Mus musculus.        

  • 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 GLUL (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Glutamine Deficiency, Congenital  (DOID:9008125)
  • 46 papers in RGD have been used to annotate Glul


    • An association has been curated linking Glul and Glutamine Deficiency, Congenital in Mus musculus.        

  • 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 GLUL (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to Glutamine Deficiency, Congenital  (DOID:9008125)
  • 46 papers in RGD have been used to annotate Glul
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:16267323


    • An association has been curated linking Glul and Glutamine Deficiency, Congenital in Mus musculus.        

  • 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 GLUL (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Glutamine Deficiency, Congenital  (DOID:9008125)
  • 46 papers in RGD have been used to annotate Glul
  • Curation Notes: ClinVar Annotator: match by term: GLUTAMINE SYNTHASE DEFICIENCY, CONGENITAL SYSTEMIC | ClinVar Annotator: match by term: Glutamine deficiency, congenital | ClinVar Annotator: match by term: Glutamine synthetase deficiency, congenital systemic
  • Original References(s): PMID:16267323 PMID:17576681 PMID:21353613 PMID:25741868 PMID:27775558 PMID:28492532 PMID:33150193 PMID:9536098


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