Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the H protein, which transfers the methylamine group of glycine from the P protein to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH). Two transcript variants, one protein-coding and the other probably not protein-coding,have been found for this gene. Also, several transcribed and non-transcribed pseudogenes of this gene exist throughout the genome.[provided by RefSeq, Jan 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| GCSHBA-20-REGO | 20 (40 μL) | 200 μL |
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| GCSHBA-20-REGR | 20 (40 μL) | 200 μL |
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| GCSHBA-20-ORGR | 20 (40 μL) | 200 μL |
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| GCSHBA-20-GOGR | 20 (40 μL) | 200 μL |
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| GCSHBA-20-GRRE | 20 (40 μL) | 200 μL |
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| GCSHBA-20-GROR | 20 (40 μL) | 200 μL |
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| GCSHBA-20-GRGO | 20 (40 μL) | 200 μL |
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| GCSHBA-20-AQOR | 20 (40 μL) | 200 μL |
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Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the H protein, which transfers the methylamine group of glycine from the P protein to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH). Two transcript variants, one protein-coding and the other probably not protein-coding,have been found for this gene. Also, several transcribed and non-transcribed pseudogenes of this gene exist throughout the genome.[provided by RefSeq, Jan 2010]
Gene Symbol : GCSH
Gene Name : Glycine cleavage system protein H
Chromosome : CHR 16: 810,963,74-810,819,46
Locus : 16q23.2
Alt. Genes : FAM13A
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