Search Results
YDR399W / HPT1
Description: Dimeric hypoxanthine-guanine phosphoribosyltransferase, catalyzes the formation of both inosine monophosphate and guanosine monophosphate; mutations in the human homolog HPRT1 can cause Lesch-Nyhan syndrome and Kelley-Seegmiller syndrome
Other Aliases: BRA6
External IDs: S000002807 (sgd),