|
Symbol Name ID |
Arsg
arylsulfatase G MGI:1921258 |
| Darker colors indicate more annotations |
| Human Phenotypes | Astigmatism |
Cataract |
Abnormality of retinal pigmentation |
Abnormal electroretinogram |
Nystagmus |
High hypermetropia |
Myopia |
Nyctalopia |
Visual impairment |
Blindness |
Visual field defect |
Progressive visual loss |
| Disease(s) Associated with ARSG | ||||||||||||
| Usher syndrome |
| Mouse Phenotypes | short photoreceptor outer segment |
retina photoreceptor degeneration |
thin retina outer nuclear layer |
decreased total retina thickness |
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| Availability | Mouse Genotype | ||||
| Arsgtm1Tdi/Arsgtm1Tdi | |||||
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 04/30/2024 MGI 6.23 |
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