Symbol Name ID |
Oat
ornithine aminotransferase MGI:97394 |
Darker colors indicate more annotations |
Human Phenotypes | Posterior subcapsular cataract |
Chorioretinal atrophy |
Foveoschisis |
Macular thickening |
Myopia |
Nyctalopia |
Visual impairment |
Blindness |
Disease(s) Associated with OAT | ||||||||
gyrate atrophy |
Mouse Phenotypes | decreased retina photoreceptor cell number |
disorganized photoreceptor inner segment |
short photoreceptor inner segment |
absent photoreceptor outer segment |
short photoreceptor outer segment |
abnormal retina pigment epithelium morphology |
retina pigment epithelium atrophy |
cataract |
abnormal retina morphology |
thin retina outer nuclear layer |
retina degeneration |
abnormal eye electrophysiology |
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Availability | Mouse Genotype | ||||||||||||
Oatrhg/Oatrhg | |||||||||||||
Oattm1Dva/Oattm1Dva | |||||||||||||
Oatrhg/Oattm1Dva |
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 03/19/2024 MGI 6.23 |
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