Description

The presence of an additional TA repeat in the TATA region of the UGT1A1 promoter (ie, 7 TA repeats; UGT1A1*28, rs8175347) markedly reduces the level of hepatic bilirubin UDP-glucuronosyltransferase 1A1 (UGT1A1), the enzyme necessary for the conjugation of bilirubin. Individuals homozygous for the UGT1A1*28 allele develop Gilbert syndrome, a condition characterized by periods of mild unconjugated hyperbilirubinemia. In addition, individuals positive for the UGT1A1*28 allele are more likely to experience severe adverse effects during irinotecan chemotherapy. Identifying a patient's genotype for the UGT1A1 allele helps determine appropriate starting dosages for irinotecan, reducing the risk of severe toxicity and improving overall therapy. Source: Regenstrief LOINC

Basic Part Properties

Part Name
UGT1A1 gene.TA repeats
Part Display Name
UGT1A1 gene TA repeats
Part Type
Component (Describes the core component or analyte measured)
Created On
2020-04-23
Construct for LOINC Short Name
UGT1A1 TA

LOINC Terminology Service (API) using HL7® FHIR® Get Info

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=LP418235-0

Language Variants Get Info

TagLanguageTranslation
zh-CNChinese (China)UGT1A1 基因.TA 重复序列
fr-FRFrench (France)UGT1A1 gène répétitions TA
nl-NLDutch (Netherlands)UGTA1-gen.TA repeats
it-ITItalian (Italy)UGT1A1, gene.TA, ripetizioni
es-ESSpanish (Spain)Repeticiones TA del gen UGT1A1
pl-PLPolish (Poland)UGT1A1 gen.TA powtórzenia
Synonyms: Powtórzenia TA w genie UGT1A1
el-GRGreek (Greece)Γονίδιο UGT1A1.επαναλήψεις ΤΑ
Synonyms: Γονίδιο UGT1A1.επαναλήψεις ΤΑ