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GENE - TERM ANNOTATION REPORT

11 Annotations Found.

An association has been curated linking Impdh1 and Leber congenital amaurosis 11 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 IMPDH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Leber congenital amaurosis 11  (DOID:0110216)
  • 16 papers in CRRD have been used to annotate Impdh1
  • Curation Notes: ClinVar Annotator: match by OMIM:613837
  • Original References(s): PMID:16384941


  • An association has been curated linking Impdh1 and Leber congenital amaurosis 11 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 IMPDH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Leber congenital amaurosis 11  (DOID:0110216)
  • 16 papers in CRRD have been used to annotate Impdh1


  • An association has been curated linking Impdh1 and Leber congenital amaurosis 11 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 IMPDH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Leber congenital amaurosis 11  (DOID:0110216)
  • 16 papers in CRRD have been used to annotate Impdh1
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis 11
  • Original References(s): PMID:25741868


  • An association has been curated linking Impdh1 and Leber congenital amaurosis 11 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 IMPDH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Leber congenital amaurosis 11  (DOID:0110216)
  • 16 papers in CRRD have been used to annotate Impdh1
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis 11


  • An association has been curated linking Impdh1 and Leber congenital amaurosis 11 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 IMPDH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Leber congenital amaurosis 11  (DOID:0110216)
  • 16 papers in CRRD have been used to annotate Impdh1
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis 11
  • Original References(s): PMID:16384941, PMID:17851563, PMID:19480389, PMID:20238057, PMID:26558346, PMID:28492532


  • An association has been curated linking Impdh1 and Leber congenital amaurosis 11 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 IMPDH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Leber congenital amaurosis 11  (DOID:0110216)
  • 16 papers in CRRD have been used to annotate Impdh1
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis 11
  • Original References(s): PMID:28492532


  • An association has been curated linking Impdh1 and Leber congenital amaurosis 11 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 IMPDH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Leber congenital amaurosis 11  (DOID:0110216)
  • 16 papers in CRRD have been used to annotate Impdh1
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis 11
  • Original References(s): PMID:20045992, PMID:28492532


  • An association has been curated linking Impdh1 and Leber congenital amaurosis 11 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 IMPDH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Leber congenital amaurosis 11  (DOID:0110216)
  • 16 papers in CRRD have been used to annotate Impdh1
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis 11
  • Original References(s): PMID:20718729


  • An association has been curated linking Impdh1 and Leber congenital amaurosis 11 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 IMPDH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Leber congenital amaurosis 11  (DOID:0110216)
  • 16 papers in CRRD have been used to annotate Impdh1
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis 11
  • Original References(s): PMID:28492532, PMID:30718709


  • An association has been curated linking Impdh1 and Leber congenital amaurosis 11 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 IMPDH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Leber congenital amaurosis 11  (DOID:0110216)
  • 16 papers in CRRD have been used to annotate Impdh1
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis 11
  • Original References(s): PMID:20718729, PMID:24244438, PMID:28492532


  • An association has been curated linking Impdh1 and Leber congenital amaurosis 11 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 IMPDH1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Leber congenital amaurosis 11  (DOID:0110216)
  • 16 papers in CRRD have been used to annotate Impdh1
  • Curation Notes: ClinVar Annotator: match by term: Leber congenital amaurosis 11
  • Original References(s): PMID:25741868, PMID:28492532


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.