|
Symbol Name ID |
Snrnp200
small nuclear ribonucleoprotein 200 (U5) MGI:2444401 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal retinal vascular morphology |
Attenuation of retinal blood vessels |
Keratoconus |
Posterior subcapsular cataract |
Optic atrophy |
Optic disc pallor |
Abnormality of retinal pigmentation |
Bone spicule pigmentation of the retina |
Retinal degeneration |
Retinal pigment epithelial atrophy |
Rod-cone dystrophy |
Abnormal electroretinogram |
Nystagmus |
Ophthalmoplegia |
Nyctalopia |
Progressive night blindness |
Photophobia |
Photopsia |
Visual impairment |
Blindness |
Peripheral visual field loss |
Glaucoma |
| Disease(s) Associated with SNRNP200 | ||||||||||||||||||||||
| retinitis pigmentosa | ||||||||||||||||||||||
| retinitis pigmentosa 33 |
| Mouse Phenotypes | impaired pupillary reflex |
exophthalmos |
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| Availability | Mouse Genotype | ||
| Snrnp200tm1b(KOMP)Mbp/Snrnp200+ | |||
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 05/14/2024 MGI 6.23 |
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