Entity Details
| Primary name |
ZP1_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | P60852 |
| EntryName | ZP1_HUMAN |
| FullName | Zona pellucida sperm-binding protein 1 |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 638 |
| SequenceStatus | complete |
| DateCreated | 2004-04-13 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Cell membrane |
| Zona pellucida |
Domains
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| Domain | Name | Category | Type |
| IPR000519 | P-type trefoil domain | Domain | Domain |
| IPR001507 | Zona pellucida domain | Domain | Domain |
| IPR017957 | P-type trefoil, conserved site | Site | Conserved site |
| IPR017977 | Zona pellucida domain, conserved site | Site | Conserved site |
Diseases
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| Disease ID | Source | Name | Description |
| 615774 | OMIM | Oocyte maturation defect 1 (OOMD1) | An infertility disorder caused by defective oocyte maturation that results in abnormal eggs lacking a zona pellucida. Affected females have normal menstrual cycles and sex hormone levels, no obstruction in the fallopian tubes or abnormalities of the uterus or adnexa. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
0 interactions
| Interactor | Partner | Sources | Publications | Link |