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Symbol
Name
ID
Oat
ornithine aminotransferase
MGI:97394
Phenotype annotations related to vision/eye
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
Availability Mouse Genotype
Oatrhg/Oatrhg
Oattm1Dva/Oattm1Dva
Oatrhg/Oattm1Dva

Contributing Projects:
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
The Jackson Laboratory