This gene encodes a protein that belongs to the CN hydrolase family. Beta-ureidopropionase catalyzes the last step in the pyrimidine degradation pathway. The pyrimidine bases uracil and thymine are degraded via the consecutive action of dihydropyrimidine dehydrogenase (DHPDH), dihydropyrimidinase (DHP) and beta-ureidopropionase (UP) to beta-alanine and beta-aminoisobutyric acid, respectively. UP deficiencies are associated with N-carbamyl-beta-amino aciduria and may lead to abnormalities in neurological activity. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| UPB1-20-RE | 20 (40 μL) | 200 μL |  |
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| UPB1-20-OR | 20 (40 μL) | 200 μL |  |
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| UPB1-20-GO | 20 (40 μL) | 200 μL |  |
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| UPB1-20-GR | 20 (40 μL) | 200 μL |  |
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| UPB1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein that belongs to the CN hydrolase family. Beta-ureidopropionase catalyzes the last step in the pyrimidine degradation pathway. The pyrimidine bases uracil and thymine are degraded via the consecutive action of dihydropyrimidine dehydrogenase (DHPDH), dihydropyrimidinase (DHP) and beta-ureidopropionase (UP) to beta-alanine and beta-aminoisobutyric acid, respectively. UP deficiencies are associated with N-carbamyl-beta-amino aciduria and may lead to abnormalities in neurological activity. [provided by RefSeq, Jul 2008]
Gene Symbol : UPB1
Gene Name : Beta-ureidopropionase 1
Chromosome : CHR 22: 244,950,59-245,286,80
Locus : 22q11.23
Alt. Genes : TRIM10
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