|
Symbol Name ID |
Agxt
alanine-glyoxylate aminotransferase MGI:1329033 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of metabolism/homeostasis |
Abnormal circulating enzyme concentration |
Reduced hepatic alanine-glyoxylate aminotransferase activity |
Metabolic acidosis |
Dehydration |
Hematuria |
Elevated urinary glycolic acid level |
Hyperoxaluria |
Calcinosis cutis |
| Disease(s) Associated with AGXT | |||||||||
| primary hyperoxaluria type 1 |
| Mouse Phenotypes | hyperoxaluria |
crystalluria |
increased physiological sensitivity to xenobiotic |
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| Availability | Mouse Genotype | |||
| Agxttm1Ull/Agxttm1Ull | ||||
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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