rs111033541
This is a variant in the UGT1A10 gene that changes a leucine to an arginine.
▶ClinVar annotation
Bilirubin, serum level of, quantitative trait locus 1 (BILIQTL1); Crigler-Najjar syndrome type 1; Crigler-Najjar syndrome, type II; Gilbert syndrome; Lucey-Driscoll syndrome (HBLRTFN)
View on ClinVar →About UGT1A10
This gene encodes a UDP-glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water-soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. The enzyme encoded by this gene has glucuronidase activity on mycophenolic acid, coumarins, and quinolines. [provided by RefSeq, Jul 2008]
View all UGT1A10 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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