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GENE - TERM ANNOTATION REPORT

10 Annotations Found.

An association has been curated linking Ugt1a5 and Hyperbilirubinemia, Transient Familial Neonatal 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 UGT1A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 9 papers in RGD have been used to annotate Ugt1a5
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia

  • This annotation was curated on 2019-08-06 05:29:04.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a5 and Hyperbilirubinemia, Transient Familial Neonatal 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 UGT1A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 9 papers in RGD have been used to annotate Ugt1a5
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:11061796, PMID:18004206, PMID:18414213, PMID:25741868

  • This annotation was curated on 2019-08-06 05:28:27.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a5 and Hyperbilirubinemia, Transient Familial Neonatal 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 UGT1A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 9 papers in RGD have been used to annotate Ugt1a5
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:15304120, PMID:25741868, PMID:25993113, PMID:26727668

  • This annotation was curated on 2019-08-06 05:24:47.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a5 and Hyperbilirubinemia, Transient Familial Neonatal 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 UGT1A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 9 papers in RGD have been used to annotate Ugt1a5
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:25741868

  • This annotation was curated on 2019-08-06 05:22:55.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a5 and Hyperbilirubinemia, Transient Familial Neonatal 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 UGT1A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 9 papers in RGD have been used to annotate Ugt1a5
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:11061796

  • This annotation was curated on 2019-08-06 05:28:28.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a5 and Hyperbilirubinemia, Transient Familial Neonatal 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 UGT1A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 9 papers in RGD have been used to annotate Ugt1a5
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:18414213, PMID:22514612

  • This annotation was curated on 2019-08-06 05:26:21.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a5 and Hyperbilirubinemia, Transient Familial Neonatal 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 UGT1A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 9 papers in RGD have been used to annotate Ugt1a5
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:11182932, PMID:15712364, PMID:18414213, PMID:22325916, PMID:23290513, PMID:26039129, PMID:26697581, PMID:26716871

  • This annotation was curated on 2019-08-06 05:26:19.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a5 and Hyperbilirubinemia, Transient Familial Neonatal 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 UGT1A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 9 papers in RGD have been used to annotate Ugt1a5
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • 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

  • This annotation was curated on 2019-08-06 05:28:26.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a5 and Hyperbilirubinemia, Transient Familial Neonatal 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 UGT1A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 9 papers in RGD have been used to annotate Ugt1a5
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:10190918, PMID:10968441, PMID:11003624, PMID:11061796, PMID:11370628, PMID:11425418, PMID:12402338, PMID:12850492, PMID:12859413, PMID:15372086, PMID:15857854, PMID:16114182, PMID:1692835, PMID:17496722, PMID:17728214, PMID:19243019, PMID:20406168, PMID:22676194, PMID:23529007, PMID:25741868, PMID:28074472, PMID:28367249, PMID:28520360, PMID:7565971, PMID:8514037, PMID:9342374, PMID:9375768, PMID:9446675, PMID:9621515, PMID:9653159

  • This annotation was curated on 2019-08-06 05:28:24.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a5 and Hyperbilirubinemia, Transient Familial Neonatal 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 UGT1A4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 9 papers in RGD have been used to annotate Ugt1a5
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:15712364, PMID:25741868

  • This annotation was curated on 2019-08-06 05:24:49.0 by RGD . For more information contact us

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