Yerevan
EN
Lab tests
18-071

UDP-glucuronosyltransferase 1A1 (UGT1A1). Detection of mutation (TA)6/7 (gene regulatory region)

Description

The marker is associated with changes in bilirubin metabolism levels. It is investigated to detect genetic predisposition to the development of Gilbert's syndrome, neonatal hyperbilirubinemia, and Crigler-Najjar syndrome. It is informative for evaluating the effectiveness of treatment with Irinotecan (Irinotel, Iriten, Irnocam, Camptera, Campto). OMIM: 191740.

Period of execution

Within 9 days

Biomaterial type

  • Venous blood
Total price
17785 ֏
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