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UGT1A1

Drugs affected by UGT1A1

UDP Glucuronosyltransferase Family 1 Member A1

6 medications 9 brand products

About UGT1A1

UGT1A1 clears bilirubin (the molecule that builds up in jaundice) and several drugs including irinotecan and nilotinib.[1] A variant called *28, common in people of all ancestries, reduces UGT1A1 activity. It's the cause of Gilbert's syndrome, a benign condition, but it also makes cancer patients much more susceptible to severe side effects from irinotecan-based chemotherapy.[2]

Oncology dosing of irinotecan is often adjusted down for patients carrying two copies of the UGT1A1*28 variant.

What we test for UGT1A1

Gene2Rx uses definitions covering 8 named UGT1A1 star alleles, built from 7 variants in Gene2Rx definitions. Results depend on the variants available in your upload.

8
Star alleles
7
Defined variants
Gene2Rx definitions
Source
GRCh38
Genome build
Normal Function 2 Increased Function 1 Decreased Function 4 Unknown Function 1

Notable UGT1A1 alleles

*1 Normal Function
Reference allele — normal UGT1A1 glucuronidation activity.
*28 Decreased Function
A decreased-function TA-repeat allele linked to Gilbert syndrome and irinotecan neutropenia.
~35% in Europeans
*6 Decreased Function
A decreased-function missense allele common in East Asian populations.
What are star alleles?

Star alleles (like *1, *2, *4) are standardized names for distinct versions of a pharmacogene. *1 is the reference; other numbers identify distinct allele definitions. A higher number does not mean lower function.

You inherit one allele from each parent, so your genotype is a pair (e.g. *1/*4). The pair determines your predicted phenotype — for example, whether you metabolize a drug at a normal, decreased, or no-function rate.

PharmVar is the international registry that defines and curates these allele names. Gene2Rx uses the supported definitions summarized here. Coverage depends on the variants present in your input; this is not a guarantee that every cataloged allele can be identified.

Medications with UGT1A1 information

This list contains 6 medications with UGT1A1 information from the sources shown below. Evidence and report eligibility differ by drug; each page explains its scope and limitations.

antiretrovirals

Brand products containing a UGT1A1-affected ingredient

These branded medications include at least one active ingredient whose metabolism or action involves UGT1A1. Each links to its full pharmacogenetic breakdown.

References

  1. U.S. Food and Drug Administration. Table of Pharmacogenomic Biomarkers in Drug Labeling (2024). fda.gov
  2. PharmGKB / Stanford University. PharmGKB: The Pharmacogenomics Knowledge Base. pharmgkb.org

Explore UGT1A1 in your report

A Gene2Rx report interprets supported variants in the context of your data and purchased report. Missing or uncertain calls may prevent an assessment.

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Informational only, not medical advice. The presence of a UGT1A1 pharmacogenetic guideline does not mean every patient needs to change their dose. Never start, stop, or change a medication without talking to your prescribing clinician.

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