This gene encodes a mitochondrial protein that catalyzes the first step in proline degradation. Mutations in this gene are associated with hyperprolinemia type 1 and susceptibility to schizophrenia 4 (SCZD4). This gene is located on chromosome 22q11.21, a region which has also been associated with the contiguous gene deletion syndromes, DiGeorge and CATCH22. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| PRODH-20-RE | 20 (40 μL) | 200 μL |  |
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| PRODH-20-OR | 20 (40 μL) | 200 μL |  |
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| PRODH-20-GO | 20 (40 μL) | 200 μL |  |
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| PRODH-20-GR | 20 (40 μL) | 200 μL |  |
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| PRODH-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a mitochondrial protein that catalyzes the first step in proline degradation. Mutations in this gene are associated with hyperprolinemia type 1 and susceptibility to schizophrenia 4 (SCZD4). This gene is located on chromosome 22q11.21, a region which has also been associated with the contiguous gene deletion syndromes, DiGeorge and CATCH22. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2010]
Gene Symbol : PRODH
Gene Name : Proline dehydrogenase 1
Chromosome : CHR 22: 189,365,52-189,127,73
Locus : 22q11.21
Alt. Genes : ACTBP9
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