Entity Details
| Primary name |
STAG3_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q9UJ98 |
| EntryName | STAG3_HUMAN |
| FullName | Cohesin subunit SA-3 |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 1225 |
| SequenceStatus | complete |
| DateCreated | 2003-03-25 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Chromosome |
| Nucleus |
Domains
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| Domain | Name | Category | Type |
| IPR013721 | STAG | Domain | Domain |
| IPR016024 | Armadillo-type fold | Family | Homologous superfamily |
| IPR020839 | Stromalin conservative domain | Domain | Domain |
| IPR039662 | Cohesin subunit Scc3/SA | Family | Family |
Diseases
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| Disease ID | Source | Name | Description |
| 615723 | OMIM | Premature ovarian failure 8 (POF8) | An ovarian disorder defined as the cessation of ovarian function under the age of 40 years. It is characterized by oligomenorrhea or amenorrhea, in the presence of elevated levels of serum gonadotropins and low estradiol. The disease is caused by variants affecting the gene represented in this entry. A homozygous deletion in STAG3 predicted to result in frameshift and premature truncation, has been shown to be the cause of premature ovarian failure in a large consanguineous family. |
Interactions
2 interactions