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
ID |
gene |
Alias |
Chr |
Start |
Stop |
Strand |
orf_classification |
YDR399W |
HPT1 |
HPT1 BRA6 HPRT |
4 |
1270061 |
1270726 |
+ |
Verified |