This gene encodes the 5-methyltetrahydrofolate-homocysteine methyltransferase. This enzyme, also known as cobalamin-dependent methionine synthase, catalyzes the final step in methionine biosynthesis. Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| MTR-20-RE | 20 (40 μL) | 200 μL |  |
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| MTR-20-OR | 20 (40 μL) | 200 μL |  |
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| MTR-20-GO | 20 (40 μL) | 200 μL |  |
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| MTR-20-GR | 20 (40 μL) | 200 μL |  |
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| MTR-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes the 5-methyltetrahydrofolate-homocysteine methyltransferase. This enzyme, also known as cobalamin-dependent methionine synthase, catalyzes the final step in methionine biosynthesis. Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, May 2014]
Gene Symbol : MTR
Gene Name : 5-methyltetrahydrofolate-homocysteine methyltransferase
Chromosome : CHR 1: 236,794,303-236,903,980
Locus : 1q43
Alt. Genes : ZNF263
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