|
Symbol Name ID |
Wdr81
WD repeat domain 81 MGI:2681828 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cataract |
Iris coloboma |
Chorioretinal coloboma |
Optic atrophy |
Macular hypoplasia |
Strabismus |
Alternating esotropia |
Nystagmus |
Gaze-evoked nystagmus |
Rotary nystagmus |
Visual impairment |
| Disease(s) Associated with WDR81 | |||||||||||
| cerebellar ataxia, mental retardation and dysequlibrium syndrome | |||||||||||
| hydrocephalus |
| Mouse Phenotypes | decreased retina photoreceptor cell number |
decreased total retina thickness |
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| Availability | Mouse Genotype | ||
| Wdr81nur5/Wdr81nur5 | |||
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 04/23/2024 MGI 6.23 |
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