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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking Lpl and Familial Hyperchylomicronemia 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 LPL (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Familial Hyperchylomicronemia Syndrome  (DOID:9002180)
  • 60 papers in CRRD have been used to annotate Lpl
  • Curation Notes: ClinVar Annotator: match by term: Hyperlipoproteinemia type 1
  • Original References(s): PMID:23246289


  • An association has been curated linking Lpl and Familial Hyperchylomicronemia 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 LPL (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Familial Hyperchylomicronemia Syndrome  (DOID:9002180)
  • 60 papers in CRRD have been used to annotate Lpl
  • Curation Notes: ClinVar Annotator: match by term: Hyperlipoproteinemia type 1
  • Original References(s): PMID:1562620, PMID:1576758, PMID:16174715, PMID:1737848


  • An association has been curated linking Lpl and Familial Hyperchylomicronemia 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 LPL (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Familial Hyperchylomicronemia Syndrome  (DOID:9002180)
  • 60 papers in CRRD have been used to annotate Lpl
  • Curation Notes: ClinVar Annotator: match by term: Hyperlipoproteinemia type 1
  • Original References(s): PMID:1598907, PMID:30311386


  • An association has been curated linking Lpl and Familial Hyperchylomicronemia 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 LPL (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Familial Hyperchylomicronemia Syndrome  (DOID:9002180)
  • 60 papers in CRRD have been used to annotate Lpl
  • Curation Notes: ClinVar Annotator: match by term: Hyperlipoproteinemia type 1
  • Original References(s): PMID:10735636, PMID:25741868


  • An association has been curated linking Lpl and Familial Hyperchylomicronemia 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 LPL (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Familial Hyperchylomicronemia Syndrome  (DOID:9002180)
  • 60 papers in CRRD have been used to annotate Lpl
  • Curation Notes: ClinVar Annotator: match by term: Hyperlipoproteinemia type 1
  • Original References(s): PMID:1731801, PMID:1907278


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