UDP Glucuronosyltransferase Family 1 Member A1
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]
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.
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.
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.
These branded medications include at least one active ingredient whose metabolism or action involves UGT1A1. Each links to its full pharmacogenetic breakdown.
A Gene2Rx report interprets supported variants in the context of your data and purchased report. Missing or uncertain calls may prevent an assessment.
Get your report Look up a medicationInformational 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.