Entity Details
| Primary name |
PDYN_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | P01213 |
| EntryName | PDYN_HUMAN |
| FullName | Proenkephalin-B |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 254 |
| SequenceStatus | complete |
| DateCreated | 1986-07-21 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Secreted |
Domains
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| Domain | Name | Category | Type |
| IPR000750 | Proenkephalin B | Family | Family |
| IPR006024 | Opioid neuropeptide precursor | Family | Family |
Diseases
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| Disease ID | Source | Name | Description |
| 610245 | OMIM | Spinocerebellar ataxia 23 (SCA23) | Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCA23 is an adult-onset autosomal dominant form characterized by slowly progressive gait and limb ataxia, with variable additional features, including peripheral neuropathy and dysarthria. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
2 interactions