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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking Nsdhl and CHILD syndrome 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 NSDHL (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to CHILD syndrome  (DOID:0111822)
  • 15 papers in RGD have been used to annotate Nsdhl


  • An association has been curated linking Nsdhl and CHILD syndrome 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 NSDHL (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to CHILD syndrome  (DOID:0111822)
  • 15 papers in RGD have been used to annotate Nsdhl
  • Curation Notes: ClinVar Annotator: match by OMIM:308050
  • Original References(s): PMID:18414213


  • An association has been curated linking Nsdhl and CHILD syndrome 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 NSDHL (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to CHILD syndrome  (DOID:0111822)
  • 15 papers in RGD have been used to annotate Nsdhl
  • Curation Notes: ClinVar Annotator: match by OMIM:308050
  • Original References(s): PMID:11907515


  • An association has been curated linking Nsdhl and CHILD syndrome 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 NSDHL (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to CHILD syndrome  (DOID:0111822)
  • 15 papers in RGD have been used to annotate Nsdhl
  • Curation Notes: ClinVar Annotator: match by OMIM:308050


  • An association has been curated linking Nsdhl and CHILD syndrome 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 NSDHL (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to CHILD syndrome  (DOID:0111822)
  • 15 papers in RGD have been used to annotate Nsdhl
  • Curation Notes: ClinVar Annotator: match by OMIM:308050
  • Original References(s): PMID:10710235


  • An association has been curated linking Nsdhl and CHILD syndrome 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 NSDHL (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to CHILD syndrome  (DOID:0111822)
  • 15 papers in RGD have been used to annotate Nsdhl
  • Curation Notes: ClinVar Annotator: match by OMIM:308050
  • Original References(s): PMID:12966526


  • An association has been curated linking Nsdhl and CHILD syndrome 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 NSDHL (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to CHILD syndrome  (DOID:0111822)
  • 15 papers in RGD have been used to annotate Nsdhl
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:25526675


  • An association has been curated linking Nsdhl and CHILD syndrome 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 NSDHL (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to CHILD syndrome  (DOID:0111822)
  • 15 papers in RGD have been used to annotate Nsdhl
  • Curation Notes: ClinVar Annotator: match by term: Child syndrome
  • Original References(s): PMID:18414213 PMID:28492532


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