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GENE - TERM ANNOTATION REPORT
RGD ID:
1583689
Species:
Rattus norvegicus
RGD Object:
Gene
Symbol:
Ugt1a5
Name:
UDP glucuronosyltransferase family 1 member A5
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 Symbol
Qualifier
Evidence
With
Reference
Source
Notes
Original Reference(s)
Ugt1a5
ISO
UGT1A4 (Homo sapiens)
8554872
ClinVar
ClinVar Annotator: match by term: Hyperbilirubinemia
PMID: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:35942604
PMID:36274106
PMID:36350824
PMID:36574877
PMID:37671043
PMID:38279097
PMID:9630669
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