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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking Wdr1 and Lazy Leukocyte 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 WDR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Lazy Leukocyte Syndrome  (DOID:9005933)
  • 5 papers in RGD have been used to annotate Wdr1


  • An association has been curated linking Wdr1 and Lazy Leukocyte 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 WDR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Lazy Leukocyte Syndrome  (DOID:9005933)
  • 5 papers in RGD have been used to annotate Wdr1
  • Curation Notes: ClinVar Annotator: match by term: Lazy leukocyte syndrome
  • Original References(s): PMID:27557945


  • An association has been curated linking Wdr1 and Lazy Leukocyte 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 WDR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Lazy Leukocyte Syndrome  (DOID:9005933)
  • 5 papers in RGD have been used to annotate Wdr1
  • Curation Notes: ClinVar Annotator: match by term: WDR1 deficiency


  • An association has been curated linking Wdr1 and Lazy Leukocyte 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 WDR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Lazy Leukocyte Syndrome  (DOID:9005933)
  • 5 papers in RGD have been used to annotate Wdr1
  • Curation Notes: ClinVar Annotator: match by term: Lazy leukocyte syndrome
  • Original References(s): PMID:29751004


  • An association has been curated linking Wdr1 and Lazy Leukocyte 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 WDR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Lazy Leukocyte Syndrome  (DOID:9005933)
  • 5 papers in RGD have been used to annotate Wdr1
  • Curation Notes: ClinVar Annotator: match by term: Lazy leukocyte syndrome
  • Original References(s): PMID:27994071


  • An association has been curated linking Wdr1 and Lazy Leukocyte 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 WDR1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Lazy Leukocyte Syndrome  (DOID:9005933)
  • 5 papers in RGD have been used to annotate Wdr1
  • Curation Notes: ClinVar Annotator: match by term: Lazy leukocyte syndrome
  • Original References(s): PMID:205284 PMID:27557945


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