Symbol Name ID |
Mocs1
molybdenum cofactor synthesis 1 MGI:1928904 |
Darker colors indicate more annotations |
Human Phenotypes | Hypouricemia |
Aldehyde oxidase deficiency |
Molybdenum cofactor deficiency |
Reduced xanthine dehydrogenase level |
Sulfite oxidase deficiency |
Increased urinary hypoxanthine level |
Decreased urinary urate |
Decreased urinary sulfate |
Absent urinary urothione |
Elevated urinary S-sulfocysteine level |
Increased urinary taurine |
Increased urinary sulfite level |
Increased urinary thiosulfate |
Xanthinuria |
Disease(s) Associated with MOCS1 | ||||||||||||||
molybdenum cofactor deficiency type A |
Mouse Phenotypes | taurinuria |
aminoaciduria |
cystinuria |
abnormal urine homeostasis |
decreased urine uric acid level |
increased urine xanthine level |
abnormal enzyme/coenzyme activity |
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Availability | Mouse Genotype | |||||||
Mocs1tm1Jre/Mocs1tm1Jre |
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 04/16/2024 MGI 6.23 |
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