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GENE - TERM ANNOTATION REPORT

14 Annotations Found.

An association has been curated linking Ugt1a1 and Gilbert syndrome in Mus musculus.        

  • 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]
  • 6 RGD objects have been annotated to Gilbert syndrome  (DOID:2739)
  • 48 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: Gilbert syndrome, susceptibility to
  • Original References(s): PMID:11906189, PMID:15378351

  • This annotation was curated on 2019-12-03 05:57:58.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a1 and Gilbert syndrome in Mus musculus.        

  • 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]
  • 6 RGD objects have been annotated to Gilbert syndrome  (DOID:2739)
  • 48 papers in RGD have been used to annotate Ugt1a1

  • This annotation was curated on 2019-12-04 19:57:07.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a1 and Gilbert syndrome in Mus musculus.        

  • 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]
  • 6 RGD objects have been annotated to Gilbert syndrome  (DOID:2739)
  • 48 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: Gilbert's syndrome
  • Original References(s): PMID:1692835, PMID:18004206, PMID:18414213, PMID:6480579, PMID:8528206, PMID:9621515

  • This annotation was curated on 2019-12-03 05:57:52.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a1 and Gilbert syndrome in Mus musculus.        

  • 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]
  • 6 RGD objects have been annotated to Gilbert syndrome  (DOID:2739)
  • 48 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: HYPERBILIRUBINEMIA, GILBERT TYPE
  • Original References(s): PMID:11061796, PMID:18004206, PMID:18414213, PMID:25741868

  • This annotation was curated on 2019-12-03 05:57:56.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a1 and Gilbert syndrome in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with UGT1A1 (Homo sapiens) [(EXP) inferred from experiment]
  • 6 RGD objects have been annotated to Gilbert syndrome  (DOID:2739)
  • 48 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:10421657, PMID:15180166, PMID:15297419

  • This annotation was curated on 2019-12-03 04:45:54.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a1 and Gilbert syndrome in Mus musculus.        

  • 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]
  • 6 RGD objects have been annotated to Gilbert syndrome  (DOID:2739)
  • 48 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: HYPERBILIRUBINEMIA, GILBERT TYPE
  • Original References(s): PMID:15304120, PMID:25741868, PMID:25993113, PMID:26727668

  • This annotation was curated on 2019-12-03 06:01:15.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a1 and Gilbert syndrome in Mus musculus.        

  • 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]
  • 6 RGD objects have been annotated to Gilbert syndrome  (DOID:2739)
  • 48 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: HYPERBILIRUBINEMIA, GILBERT TYPE
  • Original References(s): PMID:25741868

  • This annotation was curated on 2019-12-03 06:00:26.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a1 and Gilbert syndrome in Mus musculus.        

  • 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]
  • 6 RGD objects have been annotated to Gilbert syndrome  (DOID:2739)
  • 48 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: Gilbert's syndrome
  • Original References(s): PMID:14616765, PMID:1692835, PMID:8276413

  • This annotation was curated on 2019-12-03 05:57:51.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a1 and Gilbert syndrome in Mus musculus.        

  • 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]
  • 6 RGD objects have been annotated to Gilbert syndrome  (DOID:2739)
  • 48 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by OMIM:143500

  • This annotation was curated on 2019-12-03 06:00:50.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a1 and Gilbert syndrome in Mus musculus.        

  • 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]
  • 6 RGD objects have been annotated to Gilbert syndrome  (DOID:2739)
  • 48 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by OMIM:143500
  • Original References(s): PMID:18414213, PMID:22514612

  • This annotation was curated on 2019-12-03 05:57:58.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a1 and Gilbert syndrome in Mus musculus.        

  • 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]
  • 6 RGD objects have been annotated to Gilbert syndrome  (DOID:2739)
  • 48 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: HYPERBILIRUBINEMIA, GILBERT TYPE
  • Original References(s): PMID:11182932, PMID:15712364, PMID:18414213, PMID:22325916, PMID:23290513, PMID:26039129, PMID:26697581, PMID:26716871

  • This annotation was curated on 2019-12-03 05:57:57.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a1 and Gilbert syndrome in Mus musculus.        

  • 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]
  • 6 RGD objects have been annotated to Gilbert syndrome  (DOID:2739)
  • 48 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: HYPERBILIRUBINEMIA, GILBERT TYPE
  • 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 2019-12-03 05:57:54.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a1 and Gilbert syndrome in Mus musculus.        

  • 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]
  • 6 RGD objects have been annotated to Gilbert syndrome  (DOID:2739)
  • 48 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: HYPERBILIRUBINEMIA, GILBERT TYPE
  • Original References(s): PMID:15712364, PMID:25741868

  • This annotation was curated on 2019-12-03 05:56:15.0 by RGD . For more information contact us

    An association has been curated linking Ugt1a1 and Gilbert syndrome in Mus musculus.        

  • 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]
  • 6 RGD objects have been annotated to Gilbert syndrome  (DOID:2739)
  • 48 papers in RGD have been used to annotate Ugt1a1
  • Curation Notes: ClinVar Annotator: match by term: HYPERBILIRUBINEMIA, GILBERT TYPE
  • Original References(s): PMID:12402338, PMID:24492252

  • This annotation was curated on 2019-12-03 05:57:57.0 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.