Entity Details
| Primary name |
SUN5_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q8TC36 |
| EntryName | SUN5_HUMAN |
| FullName | SUN domain-containing protein 5 |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 379 |
| SequenceStatus | complete |
| DateCreated | 2003-01-17 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Golgi apparatus |
| Nucleus inner membrane |
Domains
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| Domain | Name | Category | Type |
| IPR008979 | Galactose-binding-like domain superfamily | Family | Homologous superfamily |
| IPR012919 | SUN domain | Domain | Domain |
| IPR030273 | SUN domain-containing protein 5 | Family | Family |
Diseases
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| Disease ID | Source | Name | Description |
| 617187 | OMIM | Spermatogenic failure 16 (SPGF16) | An infertility disorder caused by spermatogenesis defects and characterized by abnormally shaped spermatozoa in the semen of affected individuals. Most spermatozoa are made up of headless tails, while a small proportion has an abnormal head-tail junction. A few spermatozoa are made up of tailless heads. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
3 interactions