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GENE - TERM ANNOTATION REPORT

RGD ID: 1549728
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Ugt1a3
Name: UDP glycosyltransferase 1 family, polypeptide A3
Acc ID: DOID:2741
Term: bilirubin metabolic disorder
Definition: An inherited metabolic disorder that involves elevated levels of bilirubin resulting from disruption of bilirubin metabolism. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Hereditary_hyperbilirubinemia "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
Ugt1a3 ISOUGT1A5 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: HyperbilirubinemiaPMID:10975608 PMID:11061796 PMID:11182932 PMID:11983459 PMID:12105841 PMID:12181437 PMID:12208142 PMID:12485959 PMID:15304109 PMID:15304120 PMID:15712364 PMID:16269258 PMID:16610035 PMID:18004206 PMID:18414213 PMID:18419642 PMID:21297505 PMID:21319362 PMID:21726413 PMID:22169899 PMID:22325916 PMID:22514612 PMID:23290513 PMID:23875061 PMID:24033266 PMID:24749086 PMID:25741868 PMID:25993113 PMID:26039129 PMID:26250421 PMID:26697581 PMID:26716871 PMID:26727668 PMID:27264814 PMID:28492532 PMID:29137095 PMID:30669781 PMID:31145902 PMID:31450232 PMID:31737051 PMID:31858773 PMID:33083013 PMID:34953813 PMID:35257483 PMID:35426266 PMID:35436954 PMID:35781232 PMID:9630669
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