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PMID:18004212

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Citation

Girard, H, Lévesque, E, Bellemare, J, Journault, K, Caillier, B and Guillemette, C (2007) Genetic diversity at the UGT1 locus is amplified by a novel 3' alternative splicing mechanism leading to nine additional UGT1A proteins that act as regulators of glucuronidation activity. Pharmacogenet. Genomics 17:1077-89

Abstract

The gene UGT1 encodes phase II detoxification proteins involved in the elimination of small hydrophobic substances of both endogenous and exogenous origin. To date, nine functional UGT1A proteins are known to be produced from a single gene composed of alternative first exons shared with four common exons. Recently, a novel exon (referred to as exon 5b) was identified in the common shared region.

Links

PubMed Online version:10.1097/FPC.0b013e3282f1f118

Keywords

Alternative Splicing; Animals; Base Sequence; Cell Line; DNA Primers/genetics; DNA, Complementary/genetics; Exons; Genetic Variation; Glucuronides/metabolism; Glucuronosyltransferase/genetics; Glucuronosyltransferase/metabolism; Humans; Macaca fascicularis; Models, Genetic; Pharmacogenetics; RNA, Messenger/genetics; RNA, Messenger/metabolism; Rats; Recombinant Proteins/genetics; Recombinant Proteins/metabolism; Tissue Distribution; Transfection

Significance

Annotations

Gene product Qualifier GO Term Evidence Code with/from Aspect Extension Notes Status

HUMAN:UD11

involved_in

GO:2001030: negative regulation of cellular glucuronidation

ECO:0000314: direct assay evidence used in manual assertion

P

Seeded From UniProt

complete

Notes

See also

References

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