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GENE - TERM ANNOTATION REPORT

24 Annotations Found.

An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8563021 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:11061796


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:28900295 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:22983686 PMID:24390994


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11643207 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:23290513 PMID:25741868 PMID:28492532


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9684148 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:18414213 PMID:22514612 PMID:28492532


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9684146 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:11182932 PMID:15712364 PMID:16269258 PMID:18414213 PMID:22325916 PMID:23290513 PMID:23875061 PMID:25741868 PMID:26039129 PMID:26697581 PMID:26716871 PMID:28492532


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8563019 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:10412811 PMID:10472535 PMID:11061796 PMID:12502904 PMID:15304120 PMID:17850628 PMID:18004206 PMID:19243019 PMID:19390945 PMID:19397531 PMID:19830808 PMID:20975617 PMID:21272068 PMID:21319362 PMID:21342357 PMID:23014115 PMID:24033692 PMID:25200497 PMID:25741868 PMID:26467025 PMID:26604633 PMID:26830078 PMID:26857783 PMID:27220761 PMID:28492532 PMID:28520360 PMID:28585035 PMID:9630669 PMID:9784835 PMID:9929972


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8563020 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:11061796 PMID:11983459 PMID:12181437 PMID:12485959 PMID:15304109 PMID:15304120 PMID:18004206 PMID:18414213 PMID:18419642 PMID:21297505 PMID:21319362 PMID:22169899 PMID:24033266 PMID:24749086 PMID:25741868 PMID:26250421 PMID:28492532 PMID:29137095 PMID:9630669


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11636513 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:23875061 PMID:23997956 PMID:25741868 PMID:28492532


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10052444 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:19325249 PMID:25200497 PMID:25741868 PMID:26727668 PMID:28492532


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8563026 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:14550264 PMID:25741868 PMID:8706880


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11640742 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:23290513


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:13516025 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:15712364 PMID:18058623 PMID:25741868 PMID:28492532


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11638587 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:23099197 PMID:25741868 PMID:28492532


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10405510 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:10975608 PMID:12105841 PMID:12208142 PMID:15304120 PMID:16610035 PMID:21726413 PMID:25741868 PMID:25993113 PMID:26727668 PMID:27264814 PMID:28492532 PMID:29137095 PMID:30669781 PMID:31450232 PMID:31737051 PMID:31858773 PMID:33083013 PMID:34953813 PMID:35257483 PMID:35426266 PMID:35436954 PMID:35781232


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9684142 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:18414213 PMID:28492532


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11643761 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:23875061 PMID:25741868 PMID:28492532


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:13517845 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:23290513 PMID:25741868 PMID:26200705 PMID:28492532


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:10052090|RGD:11589652|RGD:13836242|RGD:28894799|RGD:28900037 (Homo sapiens) & RGD:10052090|RGD:11589652|RGD:13836242|RGD:28894799|RGD:28900037 (Homo sapiens) & RGD:10052090|RGD:11589652|RGD:13836242|RGD:28894799|RGD:28900037 (Homo sapiens) & RGD:10052090|RGD:11589652|RGD:13836242|RGD:28894799|RGD:28900037 (Homo sapiens) & RGD:10052090|RGD:11589652|RGD:13836242|RGD:28894799|RGD:28900037 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:28492532


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11586220|RGD:151757095 (Homo sapiens) & RGD:11586220|RGD:151757095 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:9684141|RGD:9684147 (Homo sapiens) & RGD:9684141|RGD:9684147 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:18414213 PMID:25741868 PMID:28492532


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8563027 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:11906189 PMID:15378351 PMID:25741868 PMID:32860008


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:15135757 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:16504606 PMID:16610035 PMID:19325249 PMID:22983686 PMID:23403257 PMID:23875061 PMID:25741868 PMID:28492532


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens) & RGD:11585024|RGD:11586403|RGD:11586708|RGD:11587533|RGD:11588516|RGD:11652419|RGD:13834375|RGD:13834991|RGD:13837350|RGD:28885535|RGD:28885862|RGD:28886253|RGD:28886594|RGD:28886603|RGD:28886985|RGD:28888456|RGD:28893055|RGD:28893382|RGD:28894497|RGD:28895089|RGD:28895435|RGD:28900046 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia


    • An association has been curated linking UGT1A10 and Hyperbilirubinemia, Transient Familial Neonatal in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:11583949|RGD:11643075|RGD:13212926|RGD:28895076|RGD:329952427 (Homo sapiens) & RGD:11583949|RGD:11643075|RGD:13212926|RGD:28895076|RGD:329952427 (Homo sapiens) & RGD:11583949|RGD:11643075|RGD:13212926|RGD:28895076|RGD:329952427 (Homo sapiens) & RGD:11583949|RGD:11643075|RGD:13212926|RGD:28895076|RGD:329952427 (Homo sapiens) & RGD:11583949|RGD:11643075|RGD:13212926|RGD:28895076|RGD:329952427 (Homo sapiens)
  • 10 RGD objects have been annotated to Hyperbilirubinemia, Transient Familial Neonatal  (DOID:9000599)
  • 7 papers in RGD have been used to annotate UGT1A10
  • Curation Notes: ClinVar Annotator: match by term: Transient familial neonatal hyperbilirubinemia
  • Original References(s): PMID:25741868


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