|
Symbol Name ID |
Wdr19
WD repeat domain 19 MGI:2443231 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal retinal vascular morphology |
Attenuation of retinal blood vessels |
Keratoconus |
Cataract |
Posterior subcapsular cataract |
Optic atrophy |
Optic disc pallor |
Abnormality of retinal pigmentation |
Bone spicule pigmentation of the retina |
Retinal degeneration |
Retinal dystrophy |
Rod-cone dystrophy |
Abnormal electroretinogram |
Undetectable electroretinogram |
Nystagmus |
Rotary nystagmus |
Ophthalmoplegia |
Hypermetropia |
Myopia |
Nyctalopia |
Progressive night blindness |
Photophobia |
Photopsia |
Visual impairment |
Reduced visual acuity |
Amblyopia |
Blindness |
Congenital blindness |
Severely reduced visual acuity |
Peripheral visual field loss |
Visual loss |
Progressive visual loss |
Glaucoma |
| Disease(s) Associated with WDR19 | |||||||||||||||||||||||||||||||||
| asphyxiating thoracic dystrophy 5 | |||||||||||||||||||||||||||||||||
| cranioectodermal dysplasia 4 | |||||||||||||||||||||||||||||||||
| retinitis pigmentosa | |||||||||||||||||||||||||||||||||
| Senior-Loken syndrome |
| Mouse Phenotypes | anophthalmia |
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| Availability | Mouse Genotype | |
| Wdr19twto/Wdr19twto | ||
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 08/02/2024 MGI 6.24 |
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