Entity Details
| Primary name |
DPP10_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q8N608 |
| EntryName | DPP10_HUMAN |
| FullName | Inactive dipeptidyl peptidase 10 |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 796 |
| SequenceStatus | complete |
| DateCreated | 2005-06-07 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Cell membrane |
Domains
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| Domain | Name | Category | Type |
| IPR001375 | Peptidase S9, prolyl oligopeptidase, catalytic domain | Domain | Domain |
| IPR002469 | Dipeptidylpeptidase IV, N-terminal domain | Domain | Domain |
| IPR029058 | Alpha/Beta hydrolase fold | Family | Homologous superfamily |
Diseases
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| Disease ID | Source | Name | Description |
| 600807 | OMIM | Asthma (ASTHMA) | The most common chronic disease affecting children and young adults. It is a complex genetic disorder with a heterogeneous phenotype, largely attributed to the interactions among many genes and between these genes and the environment. It is characterized by recurrent attacks of paroxysmal dyspnea, with wheezing due to spasmodic contraction of the bronchi. Disease susceptibility is associated with variants affecting the gene represented in this entry. |
Interactions
4 interactions