Entity Details
| Primary name |
HYEP_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | P07099 |
| EntryName | HYEP_HUMAN |
| FullName | Epoxide hydrolase 1 |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 455 |
| SequenceStatus | complete |
| DateCreated | 1988-04-01 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Endoplasmic reticulum membrane |
| Microsome membrane |
Domains
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| Domain | Name | Category | Type |
| IPR000073 | Alpha/beta hydrolase fold-1 | Domain | Domain |
| IPR000639 | Epoxide hydrolase-like | Family | Family |
| IPR016292 | Epoxide hydrolase | Family | Family |
| IPR029058 | Alpha/Beta hydrolase fold | Family | Homologous superfamily |
Diseases
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| Disease ID | Source | Name | Description |
| 607748 | OMIM | Familial hypercholanemia (FHCA) | A disorder characterized by elevated serum bile acid concentrations, itching, and fat malabsorption. The disease is caused by variants affecting the gene represented in this entry. |
Drugs
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| Drug | Name | Source | Type |
| DB00252 | Phenytoin | Drugbank | small molecule |
| DB00808 | Indapamide | Drugbank | small molecule |
Interactions
3 interactions