|
Symbol Name ID |
Slc26a8
solute carrier family 26, member 8 MGI:2385046 |
| Darker colors indicate more annotations |
| Human Phenotypes | Reduced sperm motility |
Male infertility |
| Disease(s) Associated with SLC26A8 | ||
| spermatogenic failure 3 |
| Mouse Phenotypes | thin sperm flagellum |
abnormal sperm midpiece morphology |
abnormal sperm annulus morphology |
abnormal sperm mitochondrial sheath morphology |
hairpin sperm flagellum |
kinked sperm flagellum |
asthenozoospermia |
impaired sperm capacitation |
male infertility |
impaired acrosome reaction |
abnormal sperm physiology |
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| Availability | Mouse Genotype | |||||||||||
| Slc26a8tm1Ggac/Slc26a8tm1Ggac | ||||||||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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