Entity Details
| Primary name |
SPATA16 |
| Entity type |
gene |
| Source |
Source Link |
Details
| PrimaryID | 83893 |
| RefseqGene | NG_021422 |
| Symbol | SPATA16 |
| Name | spermatogenesis associated 16 |
| Chromosome | 3 |
| Location | 3q26.31 |
| TaxID | 9606 |
| Status | live |
| SourceGenome | genomic |
| SourceOrigin | natural |
| CreationDate | 2001-05-06 |
| ModificationDate | 2021-06-11 |
Diseases
Show/Hide Table
| Disease ID | Source | Name | Description |
| 102530 | OMIM | Spermatogenic failure 6 (SPGF6) | An infertility disorder caused by spermatogenesis defects. The most prominent feature is the malformation of the acrosome, which can be totally absent in most severe cases. Additional features are an abnormal nuclear shape and abnormal arrangement of the mitochondria of the spermatozoon. The disease is caused by variants affecting the gene represented in this entry. An autosomal recessive variation of SPATA16 has been shown to be responsible for the disease in a consanguineous family with members homozygous for the variation. |
Interactions
1 interaction