This gene encodes a protein that catalyzes the final step in the conversion of vitamin B(12) into adenosylcobalamin (AdoCbl), a vitamin B12-containing coenzyme for methylmalonyl-CoA mutase. Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB complementation group. Alternatively spliced transcript variants have been found. [provided by RefSeq, Apr 2011]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| MMAB-20-RE | 20 (40 μL) | 200 μL |  |
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| MMAB-20-OR | 20 (40 μL) | 200 μL |  |
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| MMAB-20-GO | 20 (40 μL) | 200 μL |  |
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| MMAB-20-GR | 20 (40 μL) | 200 μL |  |
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| MMAB-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein that catalyzes the final step in the conversion of vitamin B(12) into adenosylcobalamin (AdoCbl), a vitamin B12-containing coenzyme for methylmalonyl-CoA mutase. Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB complementation group. Alternatively spliced transcript variants have been found. [provided by RefSeq, Apr 2011]
Gene Symbol : MMAB
Gene Name : Methylmalonic aciduria (cobalamin deficiency) cblB type
Chromosome : CHR 12: 109,573,552-109,553,714
Locus : 12q24.11
Alt. Genes : PREB
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