|
Symbol Name ID |
Rgr
retinal G protein coupled receptor MGI:1929473 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal retinal vascular morphology |
Attenuation of retinal blood vessels |
Keratoconus |
Posterior subcapsular cataract |
Optic atrophy |
Optic disc drusen |
Optic disc pallor |
Cystoid macular edema |
Abnormality of retinal pigmentation |
Bone spicule pigmentation of the retina |
Retinal degeneration |
Retinal atrophy |
Rod-cone dystrophy |
Abnormality of fundus pigmentation |
Photoreceptor outer segment loss on macular OCT |
Abnormal electroretinogram |
Abnormal full-field electroretinogram |
Decreased light- and dark-adapted electroretinogram amplitude |
Abnormal central response of multifocal electroretinogram |
Nystagmus |
Ophthalmoplegia |
Color vision defect |
Nyctalopia |
Progressive night blindness |
Photophobia |
Photopsia |
Visual impairment |
Reduced visual acuity |
Blindness |
Constriction of peripheral visual field |
Peripheral visual field loss |
Glaucoma |
| Disease(s) Associated with RGR | ||||||||||||||||||||||||||||||||
| retinitis pigmentosa | ||||||||||||||||||||||||||||||||
| retinitis pigmentosa 44 |
| Mouse Phenotypes | abnormal eye physiology |
abnormal eye electrophysiology |
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| Availability | Mouse Genotype | ||
| Rgrtm1Hkf/Rgrtm1Hkf | |||
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 09/30/2025 MGI 6.24 |
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