Entity Details
| Primary name |
BRDT_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q58F21 |
| EntryName | BRDT_HUMAN |
| FullName | Bromodomain testis-specific protein |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 947 |
| SequenceStatus | complete |
| DateCreated | 2006-05-30 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Nucleus |
Domains
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| Domain | Name | Category | Type |
| IPR001487 | Bromodomain | Domain | Domain |
| IPR018359 | Bromodomain, conserved site | Site | Conserved site |
| IPR027353 | NET domain | Domain | Domain |
| IPR031354 | Bromodomain protein 4, C-terminal | Domain | Domain |
| IPR036427 | Bromodomain-like superfamily | Family | Homologous superfamily |
| IPR038336 | NET domain superfamily | Family | Homologous superfamily |
| IPR043508 | Brdt, bromodomain, repeat I | Domain | Domain |
| IPR043509 | Brdt, bromodomain, repeat II | Domain | Domain |
Diseases
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| Disease ID | Source | Name | Description |
| 617644 | OMIM | Spermatogenic failure 21 (SPGF21) | An infertility disorder caused by spermatogenesis defects and characterized by acephalic spermatozoa in the semen of affected individuals. SPGF21 inheritance is autosomal recessive. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
5 interactions