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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Zap70 and severe combined immunodeficiency in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Arpaia E, etal., Cell. 1994 Mar 11;76(5):947-58.
  • The annotation has been inferred from sequence orthology with ZAP70 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Arpaia E, etal., Cell. 1994 Mar 11;76(5):947-58.
  • 490 RGD objects have been annotated to severe combined immunodeficiency  (DOID:627)
  • 10 papers in RGD have been used to annotate Zap70
  • Curation Notes: selective T-cell defect, OMIM:176947


  • An association has been curated linking Zap70 and severe combined immunodeficiency 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 ZAP70 (Homo sapiens) [(EXP) inferred from experiment]
  • 490 RGD objects have been annotated to severe combined immunodeficiency  (DOID:627)
  • 10 papers in RGD have been used to annotate Zap70
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:8202713


  • An association has been curated linking Zap70 and severe combined immunodeficiency 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 ZAP70 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 490 RGD objects have been annotated to severe combined immunodeficiency  (DOID:627)
  • 10 papers in RGD have been used to annotate Zap70
  • Curation Notes: ClinVar Annotator: match by term: Severe combined immunodeficiency disease
  • Original References(s): PMID:28492532


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