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GENE - TERM ANNOTATION REPORT

RGD ID: 70821
Species: Homo sapiens
RGD Object: Gene
Symbol: UGT1A
Name: UDP glucuronosyltransferase family 1 member A complex locus
Acc ID: DOID:2739
Term: Gilbert syndrome
Definition: A bilirubin metabolic disorder that involves elevated levels of unconjugated bilirubin as bilirubin is not being conjugated as a result of reduced glucuronyltransferase activity. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Gilbert%27s_syndrome "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)
UGT1A EXP 11554173CTDCTD Direct Evidence: marker/mechanismPMID:22213127
UGT1A IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert syndrome | ClinVar Annotator: match by term: Gilbert's syndromePMID:28492532
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: HYPERBILIRUBINEMIA, GILBERT TYPEPMID:19325249 PMID:25200497 PMID:25741868 PMID:26727668 PMID:28492532
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert syndromePMID: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
UGT1A IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert syndrome | ClinVar Annotator: match by term: Gilbert's syndrome | ClinVar Annotator: match by term: HYPERBILIRUBINEMIA, GILBERT TYPEPMID:25741868
UGT1A IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert syndrome | ClinVar Annotator: match by term: Gilbert's syndrome 
UGT1A IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert's syndrome | ClinVar Annotator: match by term: HYPERBILIRUBINEMIA, GILBERT TYPEPMID:25741868 PMID:28492532
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert's syndromePMID:23875061 PMID:23997956 PMID:25741868 PMID:28492532
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: HYPERBILIRUBINEMIA, GILBERT TYPEPMID:23099197 PMID:25741868 PMID:28492532
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert's syndromePMID:23290513
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert's syndromePMID:23290513 PMID:25741868 PMID:28492532
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert syndromePMID:23875061 PMID:25741868 PMID:28492532
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert syndromePMID:15712364 PMID:18058623 PMID:25741868 PMID:28492532
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert's syndromePMID:23290513 PMID:25741868 PMID:26200705 PMID:28492532
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert's syndromePMID:23290513 PMID:26200705 PMID:28492532
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert's syndromePMID:16504606 PMID:16610035 PMID:19325249 PMID:22983686 PMID:23403257 PMID:23875061 PMID:25741868 PMID:28492532
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert syndromePMID:28492532 PMID:31858773
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert's syndromePMID:15007088 PMID:17510208 PMID:19450125 PMID:20530282 PMID:22992668 PMID:23386248 PMID:25869015 PMID:27845419
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert's syndromePMID:22983686 PMID:24390994
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert syndromePMID:14616765 PMID:1692835 PMID:25741868 PMID:8102509 PMID:8276413
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert syndromePMID:11013440 PMID:16269258 PMID:1692835 PMID:16952560 PMID:22325916 PMID:23089802 PMID:23403257 PMID:23875061 PMID:25741868 PMID:7906695 PMID:7989045 PMID:9435989
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert's syndromePMID:11316168 PMID:12181437 PMID:14616765 PMID:15304120 PMID:1692835 PMID:18004206 PMID:18414213 PMID:19325249 PMID:24033266 PMID:25200497 PMID:25741868 PMID:25755387 PMID:28492532 PMID:29137095 PMID:30544479 PMID:31467903 PMID:6480579 PMID:7715297 PMID:8528206 PMID:9621515
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert's syndromePMID: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
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert syndromePMID: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
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert syndromePMID:11968090 PMID:25741868
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert's syndromePMID:12402338 PMID:24492252
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: HYPERBILIRUBINEMIA, GILBERT TYPEPMID:14550264 PMID:25741868 PMID:8706880
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert's syndromePMID:11906189 PMID:15378351 PMID:25741868 PMID:32860008
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert syndromePMID:19414484
UGT1A IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert's syndromePMID:18414213 PMID:25741868 PMID:28492532
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert's syndromePMID:18414213 PMID:28492532
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert syndromePMID:18414213 PMID:25741868 PMID:26716871 PMID:28492532 PMID:31145902
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert's syndromePMID:11182932 PMID:15712364 PMID:16269258 PMID:18414213 PMID:22325916 PMID:23290513 PMID:23875061 PMID:25741868 PMID:26039129 PMID:26697581 PMID:26716871 PMID:28492532
UGT1A IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Gilbert's syndromePMID:18414213 PMID:22514612 PMID:28492532
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