Aliases for UGT2B17 Gene
External Ids for UGT2B17 Gene
This gene encodes a member of the uridine diphosphoglucuronosyltransferase protein family. The encoded enzyme catalyzes the transfer of glucuronic acid from uridine diphosphoglucuronic acid to a diverse array of substrates including steroid hormones and lipid-soluble drugs. This process, known as glucuronidation, is an intermediate step in the metabolism of steroids. Copy number variation in this gene is associated with susceptibility to osteoporosis.[provided by RefSeq, Apr 2010]
GeneCards Summary for UGT2B17 Gene
UGT2B17 (UDP Glucuronosyltransferase 2 Family, Polypeptide B17) is a Protein Coding gene. Diseases associated with UGT2B17 include bone mineral density qtl 12, osteoporosis and osteoporosis. Among its related pathways are Metabolism and Metabolism. GO annotations related to this gene include glucuronosyltransferase activity and retinoic acid binding. An important paralog of this gene is UGT2B15.
UniProtKB/Swiss-Prot for UGT2B17 Gene
UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. The major substrates of this isozyme are eugenol > 4-methylumbelliferone > dihydrotestosterone (DHT) > androstane-3-alpha,17-beta-diol (3-alpha-diol) > testosterone > androsterone (ADT)