Entity Details
| Primary name |
S39A4_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q6P5W5 |
| EntryName | S39A4_HUMAN |
| FullName | Zinc transporter ZIP4 |
| TaxID | 9606 |
| Evidence | evidence at transcript level |
| Length | 647 |
| SequenceStatus | complete |
| DateCreated | 2005-10-25 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Cell membrane |
| Recycling endosome membrane |
Domains
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| Domain | Name | Category | Type |
| IPR003689 | Zinc/iron permease | Family | Family |
| IPR041137 | Zinc transporter ZIP4, N-terminal | Domain | Domain |
Diseases
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| Disease ID | Source | Name | Description |
| 201100 | OMIM | Acrodermatitis enteropathica, zinc-deficiency type (AEZ) | A rare autosomal recessive disease caused by the inability to absorb sufficient zinc. The clinical features are growth retardation, immune-system dysfunction, alopecia, severe dermatitis, diarrhea and occasionally mental disorders. The disease is caused by variants affecting the gene represented in this entry. |
Drugs
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| Drug | Name | Source | Type |
| DB14533 | Zinc chloride | Drugbank | small molecule |
| DB14548 | Zinc sulfate, unspecified form | Drugbank | small molecule |
Interactions
1 interaction