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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking Htra1 and CADASIL 2 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 HTRA1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to CADASIL 2  (DOID:0111036)
  • 26 papers in RGD have been used to annotate Htra1
  • Curation Notes: ClinVar Annotator: match by term: Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
  • Original References(s): PMID:25741868


  • An association has been curated linking Htra1 and CADASIL 2 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 HTRA1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to CADASIL 2  (DOID:0111036)
  • 26 papers in RGD have been used to annotate Htra1
  • Curation Notes: ClinVar Annotator: match by term: Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
  • Original References(s): PMID:26063658


  • An association has been curated linking Htra1 and CADASIL 2 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 HTRA1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to CADASIL 2  (DOID:0111036)
  • 26 papers in RGD have been used to annotate Htra1
  • Curation Notes: ClinVar Annotator: match by term: Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
  • Original References(s): PMID:25741868, PMID:30981321


  • An association has been curated linking Htra1 and CADASIL 2 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 HTRA1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to CADASIL 2  (DOID:0111036)
  • 26 papers in RGD have been used to annotate Htra1


  • An association has been curated linking Htra1 and CADASIL 2 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 HTRA1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to CADASIL 2  (DOID:0111036)
  • 26 papers in RGD have been used to annotate Htra1
  • Curation Notes: ClinVar Annotator: match by term: Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2
  • Original References(s): PMID:19387015, PMID:25741868, PMID:26063658, PMID:32101834, PMID:32581362


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