Entity Details
| Primary name |
QRICH2 |
| Entity type |
gene |
| Source |
Source Link |
Details
| PrimaryID | 84074 |
| RefseqGene | |
| Symbol | QRICH2 |
| Name | glutamine rich 2 |
| Chromosome | 17 |
| Location | 17q25.1 |
| TaxID | 9606 |
| Status | live |
| SourceGenome | genomic |
| SourceOrigin | natural |
| CreationDate | 2001-05-27 |
| ModificationDate | 2021-06-11 |
Diseases
Show/Hide Table
| Disease ID | Source | Name | Description |
| 618341 | OMIM | Spermatogenic failure 35 (SPGF35) | An autosomal recessive infertility disorder caused by spermatogenesis defects that result in multiple abnormalities of sperm flagellum and severely impaired spermatozoa motility. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
11 interactions