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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking Ocln and pseudo-TORCH 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 OCLN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudo-TORCH syndrome 1  (DOID:0050656)
  • 20 papers in RGD have been used to annotate Ocln
  • Curation Notes: ClinVar Annotator: match by OMIM:251290


  • An association has been curated linking Ocln and pseudo-TORCH syndrome 1 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 OCLN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudo-TORCH syndrome 1  (DOID:0050656)
  • 20 papers in RGD have been used to annotate Ocln


  • An association has been curated linking Ocln and pseudo-TORCH 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 OCLN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudo-TORCH syndrome 1  (DOID:0050656)
  • 20 papers in RGD have been used to annotate Ocln
  • Curation Notes: ClinVar Annotator: match by OMIM:251290
  • Original References(s): PMID:25741868


  • An association has been curated linking Ocln and pseudo-TORCH 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 OCLN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudo-TORCH syndrome 1  (DOID:0050656)
  • 20 papers in RGD have been used to annotate Ocln
  • Curation Notes: ClinVar Annotator: match by OMIM:251290
  • Original References(s): PMID:18414213


  • An association has been curated linking Ocln and pseudo-TORCH 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 OCLN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudo-TORCH syndrome 1  (DOID:0050656)
  • 20 papers in RGD have been used to annotate Ocln
  • Curation Notes: ClinVar Annotator: match by OMIM:251290
  • Original References(s): PMID:20727516


  • An association has been curated linking Ocln and pseudo-TORCH 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 OCLN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudo-TORCH syndrome 1  (DOID:0050656)
  • 20 papers in RGD have been used to annotate Ocln
  • Curation Notes: ClinVar Annotator: match by null
  • Original References(s): PMID:19012351 PMID:20727516


  • An association has been curated linking Ocln and pseudo-TORCH 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 OCLN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to pseudo-TORCH syndrome 1  (DOID:0050656)
  • 20 papers in RGD have been used to annotate Ocln
  • Curation Notes: ClinVar Annotator: match by term: Band-like calcification with simplified gyration and polymicrogyria
  • Original References(s): PMID:20727516 PMID:25741868


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