Symbol Name ID |
Oat
ornithine aminotransferase MGI:97394 |
Darker colors indicate more annotations |
Human Phenotypes | Hyperornithinemia |
Disease(s) Associated with OAT | |
gyrate atrophy |
Mouse Phenotypes | decreased circulating arginine level |
abnormal circulating amino acid level |
decreased circulating citrulline level |
decreased circulating ornithine level |
increased circulating ornithine level |
decreased circulating phenylalanine level |
increased circulating ammonia level |
decreased circulating thyroxine level |
decreased circulating alkaline phosphatase level |
decreased circulating amylase level |
decreased circulating serum albumin level |
oroticaciduria |
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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 04/23/2024 MGI 6.23 |
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