|
Symbol Name ID |
Sod1
superoxide dismutase 1, soluble MGI:98351 |
| Darker colors indicate more annotations |
| Human Phenotypes | Blepharitis |
Abnormal retinal vascular morphology |
Attenuation of retinal blood vessels |
Keratoconus |
Cataract |
Posterior subcapsular cataract |
Nuclear cataract |
Brushfield spots |
Optic atrophy |
Optic disc pallor |
Abnormality of retinal pigmentation |
Bone spicule pigmentation of the retina |
Retinal degeneration |
Abnormal electroretinogram |
Strabismus |
Nystagmus |
Ophthalmoplegia |
Myopia |
Diplopia |
Color vision defect |
Nyctalopia |
Progressive night blindness |
Photophobia |
Photopsia |
Visual impairment |
Amblyopia |
Blindness |
Peripheral visual field loss |
Glaucoma |
| Disease(s) Associated with SOD1 | |||||||||||||||||||||||||||||
| cataract | |||||||||||||||||||||||||||||
| Down syndrome | |||||||||||||||||||||||||||||
| Parkinson's disease | |||||||||||||||||||||||||||||
| retinitis pigmentosa |
| Mouse Phenotypes | abnormal Meibomian gland morphology |
abnormal Meibomian gland acinus morphology |
Meibomian gland inflammation |
blepharitis |
decreased retina ganglion cell number |
short retina rod cell outer segment |
retina photoreceptor degeneration |
abnormal corneal epithelium morphology |
abnormal retina ganglion layer morphology |
thin retina inner nuclear layer |
disorganized retina inner nuclear layer |
abnormal retina nerve fiber layer morphology |
thin retina outer nuclear layer |
disorganized retina outer nuclear layer |
decreased a-wave amplitude |
decreased b-wave amplitude |
abnormal eye electrophysiology |
abnormal tear production |
decreased tear production |
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| Availability | Mouse Genotype | |||||||||||||||||||
| Sod1tm1Leb/Sod1tm1Leb | ||||||||||||||||||||
| Tg(Sod1*G86R)M1Jwg/0 | ||||||||||||||||||||
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 04/16/2024 MGI 6.23 |
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