<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rodriguez-Antona C</submitter><funding>Ontario Institute for Cancer Research</funding><funding>Kungliga Tekniska Högskolan</funding><funding>Vetenskapsrådet</funding><funding>Erzincan Üniversitesi</funding><funding>Robert Bosch Stiftung</funding><funding>NHGRI NIH HHS</funding><funding>McGill University</funding><funding>National Institutes of Health</funding><funding>National Human Genome Research Institute</funding><funding>NIGMS NIH HHS</funding><pagination>1159-1171</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9399309</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>112(6)</volume><pubmed_abstract>The Pharmacogene Variation Consortium (PharmVar) catalogs star (*) allele nomenclature for the polymorphic human CYP3A5 gene. Genetic variation within the CYP3A5 gene locus impacts the metabolism of several clinically important drugs, including the immunosuppressants tacrolimus, sirolimus, cyclosporine, and the benzodiazepine midazolam. Variable CYP3A5 activity is of clinical importance regarding tacrolimus metabolism. This GeneFocus provides a CYP3A5 gene summary with a focus on aspects regarding standardized nomenclature. In addition, this review also summarizes recent changes and updates, including the retirement of several allelic variants and provides an overview of how PharmVar CYP3A5 star allele nomenclature is utilized by the Pharmacogenomics Knowledgebase (PharmGKB) and the Clinic</pubmed_abstract><journal>Clinical pharmacology and therapeutics</journal><pubmed_title>PharmVar GeneFocus: CYP3A5.</pubmed_title><pmcid>PMC9399309</pmcid><funding_grant_id>2016‐01154</funding_grant_id><funding_grant_id>875510</funding_grant_id><funding_grant_id>2016‐01153</funding_grant_id><funding_grant_id>U24 HG010615</funding_grant_id><funding_grant_id>R35 GM140845</funding_grant_id><funding_grant_id>U01 HG010245</funding_grant_id><funding_grant_id>2019‐01837</funding_grant_id><pubmed_authors>Boone EC</pubmed_authors><pubmed_authors>Whirl-Carrillo M</pubmed_authors><pubmed_authors>Gilep AA</pubmed_authors><pubmed_authors>Klein TE</pubmed_authors><pubmed_authors>Rodriguez-Antona C</pubmed_authors><pubmed_authors>Drogemoller BI</pubmed_authors><pubmed_authors>Savieo JL</pubmed_authors><pubmed_authors>Wang D</pubmed_authors><pubmed_authors>van Schaik RHN</pubmed_authors><pubmed_authors>Peter AP</pubmed_authors><pubmed_authors>Gaedigk A</pubmed_authors><pubmed_authors>Ramey BE</pubmed_authors><pubmed_authors>Sangkuhl K</pubmed_authors><pubmed_authors>Pratt VM</pubmed_authors><pubmed_authors>Lauschke VM</pubmed_authors></additional><is_claimable>false</is_claimable><name>PharmVar GeneFocus: CYP3A5.</name><description>The Pharmacogene Variation Consortium (PharmVar) catalogs star (*) allele nomenclature for the polymorphic human CYP3A5 gene. Genetic variation within the CYP3A5 gene locus impacts the metabolism of several clinically important drugs, including the immunosuppressants tacrolimus, sirolimus, cyclosporine, and the benzodiazepine midazolam. Variable CYP3A5 activity is of clinical importance regarding tacrolimus metabolism. This GeneFocus provides a CYP3A5 gene summary with a focus on aspects regarding standardized nomenclature. In addition, this review also summarizes recent changes and updates, including the retirement of several allelic variants and provides an overview of how PharmVar CYP3A5 star allele nomenclature is utilized by the Pharmacogenomics Knowledgebase (PharmGKB) and the Clinic</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-05-29T21:47:07.797Z</modification><creation>2025-02-19T01:16:58.323Z</creation></dates><accession>S-EPMC9399309</accession><cross_references><pubmed>35202484</pubmed><doi>10.1002/cpt.2563</doi></cross_references></HashMap>