Entity Details
| Primary name |
QRIC2_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q9H0J4 |
| EntryName | QRIC2_HUMAN |
| FullName | Glutamine-rich protein 2 |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 1663 |
| SequenceStatus | complete |
| DateCreated | 2007-07-24 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Cell projection |
| Cytoplasm |
| Nucleus |
| Nucleus membrane |
Domains
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| Domain | Name | Category | Type |
| IPR032013 | Protein of unknown function DUF4795 | Family | Family |
Diseases
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| Disease ID | Source | Name | Description |
| 618341 | OMIM | Spermatogenic failure 35 (SPGF35) | An autosomal recessive infertility disorder caused by spermatogenesis defects that result in multiple abnormalities of sperm flagellum and severely impaired spermatozoa motility. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
3 interactions