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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Zfp592 and Galloway-Mowat syndrome 1 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 ZNF592 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Galloway-Mowat syndrome 1  (DOID:0060364)
  • 4 papers in RGD have been used to annotate Zfp592
  • Curation Notes: ClinVar Annotator: match by term: Galloway-Mowat syndrome 1


  • An association has been curated linking Zfp592 and Galloway-Mowat syndrome 1 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 ZNF592 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Galloway-Mowat syndrome 1  (DOID:0060364)
  • 4 papers in RGD have been used to annotate Zfp592
  • Curation Notes: ClinVar Annotator: match by term: Galloway-Mowat syndrome 1
  • Original References(s): PMID:25741868


  • An association has been curated linking Zfp592 and Galloway-Mowat syndrome 1 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 ZNF592 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 3 RGD objects have been annotated to Galloway-Mowat syndrome 1  (DOID:0060364)
  • 4 papers in RGD have been used to annotate Zfp592
  • Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia autosomal recessive 5
  • Original References(s): PMID:12030328 PMID:20531441 PMID:26123727


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