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GENE - TERM ANNOTATION REPORT

12 Annotations Found.

An association has been curated linking Ugt1a1 and Crigler Najjar Syndrome, Type 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 UGT1A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 79 papers in RGD have been used to annotate Ugt1a1


  • An association has been curated linking Ugt1a1 and Crigler Najjar Syndrome, Type 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 UGT1A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 79 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by OMIM:606785
  • Original References(s): PMID:11370628


  • An association has been curated linking Ugt1a1 and Crigler Najjar Syndrome, Type 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 UGT1A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 79 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by OMIM:606785
  • Original References(s): PMID:14550264 PMID:8706880


  • An association has been curated linking Ugt1a1 and Crigler Najjar Syndrome, Type 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 UGT1A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 79 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: Crigler-Najjar syndrome, type II
  • Original References(s): PMID:1692835 PMID:805737 PMID:8276413


  • An association has been curated linking Ugt1a1 and Crigler Najjar Syndrome, Type 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 UGT1A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 79 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: HYPERBILIRUBINEMIA, CRIGLER-NAJJAR TYPE II
  • Original References(s): PMID:11061796 PMID:18004206 PMID:18414213 PMID:25741868


  • An association has been curated linking Ugt1a1 and Crigler Najjar Syndrome, Type 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 UGT1A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 79 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: Crigler-Najjar syndrome, type II
  • Original References(s): PMID:1692835 PMID:18004206 PMID:18414213 PMID:28492532 PMID:6480579 PMID:8528206 PMID:9621515


  • An association has been curated linking Ugt1a1 and Crigler Najjar Syndrome, Type 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 UGT1A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 79 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: HYPERBILIRUBINEMIA, CRIGLER-NAJJAR TYPE II
  • Original References(s): PMID:15712364 PMID:25741868


  • An association has been curated linking Ugt1a1 and Crigler Najjar Syndrome, Type 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 UGT1A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 79 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: Crigler-Najjar syndrome, type II
  • Original References(s): PMID:17229650


  • An association has been curated linking Ugt1a1 and Crigler Najjar Syndrome, Type 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 UGT1A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 79 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: HYPERBILIRUBINEMIA, CRIGLER-NAJJAR TYPE II
  • Original References(s): PMID:12402338 PMID:24492252


  • An association has been curated linking Ugt1a1 and Crigler Najjar Syndrome, Type 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 UGT1A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 79 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: HYPERBILIRUBINEMIA, CRIGLER-NAJJAR TYPE II
  • Original References(s): PMID:10412811 PMID:10472535 PMID:11061796 PMID:11156391 PMID:12181437 PMID:12502904 PMID:15304120 PMID:16636344 PMID:17627617 PMID:17850628 PMID:18004206 PMID:18221820 PMID:19243019 PMID:19299905 PMID:19390945 PMID:22992668 PMID:23014115 PMID:24033692 PMID:24308720 PMID:24448639 PMID:24519753 PMID:25285015 PMID:25741868 PMID:26229432 PMID:26604633 PMID:26830078 PMID:26857783 PMID:26862009 PMID:27220761 PMID:27385990 PMID:28367249 PMID:28520360 PMID:28585035 PMID:9784835 PMID:9929972


  • An association has been curated linking Ugt1a1 and Crigler Najjar Syndrome, Type 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 UGT1A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 79 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:23875061 PMID:25741868


  • An association has been curated linking Ugt1a1 and Crigler Najjar Syndrome, Type 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 UGT1A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Crigler Najjar Syndrome, Type 2  (DOID:9001862)
  • 79 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: Crigler Najjar syndrome, type 2
  • Original References(s): PMID:12208142 PMID:15304120 PMID:25741868 PMID:25993113 PMID:26727668 PMID:28492532


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