|
Symbol Name ID |
Rlbp1
retinaldehyde binding protein 1 MGI:97930 |
| 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 |
Macular degeneration |
Abnormality of retinal pigmentation |
Bone spicule pigmentation of the retina |
Retinal degeneration |
Retinal dystrophy |
Fundus albipunctatus |
Retinal flecks |
Abnormal electroretinogram |
Nystagmus |
Ophthalmoplegia |
Color vision defect |
Nyctalopia |
Progressive night blindness |
Photophobia |
Photopsia |
Visual impairment |
Reduced visual acuity |
Blindness |
Peripheral visual field loss |
Scotoma |
Central scotoma |
Ring scotoma |
Glaucoma |
| Disease(s) Associated with RLBP1 | |||||||||||||||||||||||||||||
| Bothnia retinal dystrophy | |||||||||||||||||||||||||||||
| fundus albipunctatus | |||||||||||||||||||||||||||||
| Newfoundland cone-rod dystrophy | |||||||||||||||||||||||||||||
| retinitis pigmentosa |
| Mouse Phenotypes | decreased retina photoreceptor cell number |
retina degeneration |
abnormal eye physiology |
delayed dark adaptation |
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| Availability | Mouse Genotype | ||||
| Rlbp1tm1Jsa/Rlbp1tm1Jsa | |||||
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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