Title : Three-dimensional polyacrylamide gel-based DNA microarray method effectively identifies UDP-glucuronosyltransferase 1A1 gene polymorphisms for the correct diagnosis of Gilbert's syndrome.

Pub. Date : 2016 Mar

PMID : 26781906






1 Functional Relationships(s)
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Protein Name
Organism
1 The T-3279G mutation in the phenobarbital responsive enhancer module (PBREM), the TA-insertion in the TATA box, creating the A(TA)7TAA motif instead of A(TA)6TAA and the G211A mutation in coding exon 1, particularly in Asian populations, of the human UGT1A1 gene are the three common genotypes found in patients with Gilbert"s syndrome. Phenobarbital UDP glucuronosyltransferase family 1 member A1 Homo sapiens