| Gene Symbol | OPLAH |
| Entrez Gene ID | 26873 |
| Full Name | 5-oxoprolinase, ATP-hydrolysing |
| Synonyms | 5-Opase,OPLA,OPLAHD |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | The protein encoded by this gene acts as a homodimer, using ATP hydrolysis to catalyze the conversion of 5-oxo-L-proline to L-glutamate. Defects in this gene are a cause of 5-oxoprolinase deficiency (OPLAHD). [provided by RefSeq, Jun 2012]. |
| Disorder MIM: | |
| Disorder Html: | 5-oxoprolinase deficiency, 260005 (3) |







































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