Entity Details
| Primary name |
PMFBP_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q8TBY8 |
| EntryName | PMFBP_HUMAN |
| FullName | Polyamine-modulated factor 1-binding protein 1 |
| TaxID | 9606 |
| Evidence | evidence at transcript level |
| Length | 1007 |
| SequenceStatus | complete |
| DateCreated | 2007-09-11 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Cell projection |
Domains
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| Domain | Name | Category | Type |
| IPR037391 | Polyamine-modulated factor 1-binding protein 1 | Family | Family |
Diseases
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| Disease ID | Source | Name | Description |
| 618112 | OMIM | Spermatogenic failure 31 (SPGF31) | An autosomal recessive infertility disorder caused by spermatogenesis defects that result in oligozoospermia with a high proportion of acephalic sperm. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
3 interactions