Entity Details
Primary name |
SLC26A8 |
Entity type |
gene |
Source |
Source Link |
Details
PrimaryID | 116369 |
RefseqGene | NG_033897 |
Symbol | SLC26A8 |
Name | solute carrier family 26 member 8 |
Chromosome | 6 |
Location | 6p21.31 |
TaxID | 9606 |
Status | live |
SourceGenome | genomic |
SourceOrigin | natural |
CreationDate | 2001-10-04 |
ModificationDate | 2021-06-11 |
Diseases
Show/Hide Table
Disease ID | Source | Name | Description |
606766 | OMIM | Spermatogenic failure 3 (SPGF3) | A disorder characterized by primary infertility, sperm morphologic abnormalities, and moderate to severe asthenozoospermia, condition in which the percentage of progressively motile sperm is abnormally low. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
3 interactions