This is a nuclear gene encoding a mitochondrial enzyme that catalyzes the conversion of 5-phosphonooxy-L-lysine to ammonia, inorganic phosphate, and 2-aminoadipate semialdehyde. Mutations in this gene may cause phosphohydroxylysinuria. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| PHYKPL-20-RE | 20 (40 μL) | 200 μL |  |
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| PHYKPL-20-OR | 20 (40 μL) | 200 μL |  |
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| PHYKPL-20-GO | 20 (40 μL) | 200 μL |  |
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| PHYKPL-20-GR | 20 (40 μL) | 200 μL |  |
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| PHYKPL-20-AQ | 20 (40 μL) | 200 μL |  |
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This is a nuclear gene encoding a mitochondrial enzyme that catalyzes the conversion of 5-phosphonooxy-L-lysine to ammonia, inorganic phosphate, and 2-aminoadipate semialdehyde. Mutations in this gene may cause phosphohydroxylysinuria. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]
Gene Symbol : PHYKPL
Gene Name : 5-phosphohydroxy-L-lysine phospho-lyase
Chromosome : CHR 5: 178,232,821-178,208,473
Locus : 5q35.3
Alt. Genes : ZNF263
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