Entity Details
| Primary name |
FSIP2_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q5CZC0 |
| EntryName | FSIP2_HUMAN |
| FullName | Fibrous sheath-interacting protein 2 |
| TaxID | 9606 |
| Evidence | evidence at transcript level |
| Length | 6907 |
| SequenceStatus | complete |
| DateCreated | 2008-04-29 |
| DateModified | 2021-06-02 |
Subcellular Location
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Domains
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| Domain | Name | Category | Type |
| IPR031554 | Fibrous sheath-interacting protein 2, C-terminal | Domain | Domain |
| IPR038891 | Fibrous sheath-interacting protein 2 | Family | Family |
Diseases
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| Disease ID | Source | Name | Description |
| 618153 | OMIM | Spermatogenic failure 34 (SPGF34) | An autosomal recessive infertility disorder caused by spermatogenesis defects that result in multiple abnormalities of sperm flagellum, including irregular-caliber, short, coiled, or absent flagella. The disease may be caused by variants affecting the gene represented in this entry. |
Interactions
1 interaction