Entity Details
| Primary name |
S45A1_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q9Y2W3 |
| EntryName | S45A1_HUMAN |
| FullName | Proton-associated sugar transporter A |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 782 |
| SequenceStatus | complete |
| DateCreated | 2003-10-24 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Membrane |
Domains
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| Domain | Name | Category | Type |
| IPR011701 | Major facilitator superfamily | Family | Family |
| IPR036259 | MFS transporter superfamily | Family | Homologous superfamily |
Diseases
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| Disease ID | Source | Name | Description |
| 617532 | OMIM | Intellectual developmental disorder with neuropsychiatric features (IDDNPF) | An autosomal recessive disorder characterized by moderate to severe intellectual disability, epilepsy, and variable neuropsychiatric features, such as anxiety, obsessive-compulsive behavior, and autistic features. Mild facial dysmorphism may also be present. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
1 interaction