|
Symbol Name ID |
Impg1
interphotoreceptor matrix proteoglycan 1 MGI:1926876 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal retinal vascular morphology |
Attenuation of retinal blood vessels |
Abnormality of the eye |
Keratoconus |
Posterior subcapsular cataract |
Iris hypopigmentation |
Choroideremia |
Optic atrophy |
Optic disc pallor |
Cystoid macular degeneration |
Vitelliform-like macular lesions |
Abnormality of retinal pigmentation |
Bone spicule pigmentation of the retina |
Retinal degeneration |
Retinal nonattachment |
Abnormal electroretinogram |
Nystagmus |
Ophthalmoplegia |
Abnormality of vision |
Color vision defect |
Metamorphopsia |
Nyctalopia |
Progressive night blindness |
Photophobia |
Photopsia |
Visual impairment |
Blindness |
Visual field defect |
Peripheral visual field loss |
Glaucoma |
| Disease(s) Associated with IMPG1 | ||||||||||||||||||||||||||||||
| retinitis pigmentosa | ||||||||||||||||||||||||||||||
| vitelliform macular dystrophy |
| Mouse Phenotypes | vision/eye phenotype |
abnormal photoreceptor outer segment morphology |
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| Availability | Mouse Genotype | ||
| Impg1em1Visu/Impg1em1Visu | * | ||
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 06/12/2024 MGI 6.13 |
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