|
Symbol Name ID |
Naglu
alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB) MGI:1351641 |
| Darker colors indicate more annotations |
| Human Phenotypes | Opacification of the corneal stroma |
Corneal opacity |
Cataract |
Optic atrophy |
Pigmentary retinopathy |
Retinal degeneration |
Rod-cone dystrophy |
Nystagmus |
Myopia |
Nyctalopia |
Blindness |
Constriction of peripheral visual field |
| Disease(s) Associated with NAGLU | ||||||||||||
| Charcot-Marie-Tooth disease axonal type 2V | ||||||||||||
| mucopolysaccharidosis III |
| Mouse Phenotypes | short photoreceptor outer segment |
abnormal retina pigment epithelium morphology |
abnormal retina morphology |
thin retina outer nuclear layer |
abnormal sclera morphology |
abnormal eye electrophysiology |
abnormal rod electrophysiology |
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| Availability | Mouse Genotype | |||||||
| Naglutm1Efn/Naglutm1Efn | ||||||||
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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