This gene encodes a member of the ferredoxin-NADP(+) reductase (FNR) family of electron transferases. This protein functions in the synthesis of methionine by regenerating methionine synthase to a functional state. Because methionine synthesis requires methyl-group transfer by a folate donor, activity of the encoded enzyme is important for folate metabolism and cellular methylation. Mutations in this gene can cause homocystinuria-megaloblastic anemia, cbl E type. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2015]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| MTRR-20-RE | 20 (40 μL) | 200 μL |  |
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| MTRR-20-OR | 20 (40 μL) | 200 μL |  |
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| MTRR-20-GO | 20 (40 μL) | 200 μL |  |
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| MTRR-20-GR | 20 (40 μL) | 200 μL |  |
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| MTRR-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the ferredoxin-NADP(+) reductase (FNR) family of electron transferases. This protein functions in the synthesis of methionine by regenerating methionine synthase to a functional state. Because methionine synthesis requires methyl-group transfer by a folate donor, activity of the encoded enzyme is important for folate metabolism and cellular methylation. Mutations in this gene can cause homocystinuria-megaloblastic anemia, cbl E type. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2015]
Gene Symbol : MTRR
Gene Name : 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
Chromosome : CHR 5: 786,910,3-790,112,3
Locus : 5p15.31
Alt. Genes : PREB
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