|
Symbol Name ID |
Atxn7
ataxin 7 MGI:2179277 |
| Darker colors indicate more annotations |
| Human Phenotypes | Optic atrophy |
Macular degeneration |
Pigmentary retinopathy |
Nystagmus |
Slow saccadic eye movements |
Supranuclear ophthalmoplegia |
Progressive visual loss |
| Disease(s) Associated with ATXN7 | |||||||
| spinocerebellar ataxia 7 |
| Mouse Phenotypes | decreased retina photoreceptor cell number |
short photoreceptor outer segment |
abnormal retina rod cell morphology |
retina photoreceptor degeneration |
blepharoptosis |
thin retina inner plexiform layer |
retina outer nuclear layer degeneration |
|
| Availability | Mouse Genotype | |||||||
| Atxn7tm1Hzo/Atxn7tm1Hzo | ||||||||
| Atxn7tm1Hzo/Atxn7+ | ||||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 03/24/2026 MGI 6.24 |
|
|
|
||