The EPM2A gene, which encodes laforin, is mutated in an autosomal recessive form of adolescent progressive myoclonus epilepsy. The protein encoded by this gene binds to laforin, but its function is not known. This gene is intronless. [provided by RefSeq, Oct 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| EPM2AIP1-20-RE | 20 (40 μL) | 200 μL |  |
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| EPM2AIP1-20-OR | 20 (40 μL) | 200 μL |  |
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| EPM2AIP1-20-GO | 20 (40 μL) | 200 μL |  |
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| EPM2AIP1-20-GR | 20 (40 μL) | 200 μL |  |
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| EPM2AIP1-20-AQ | 20 (40 μL) | 200 μL |  |
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The EPM2A gene, which encodes laforin, is mutated in an autosomal recessive form of adolescent progressive myoclonus epilepsy. The protein encoded by this gene binds to laforin, but its function is not known. This gene is intronless. [provided by RefSeq, Oct 2008]
Gene Symbol : EPM2AIP1
Gene Name : EPM2A interacting protein 1
Chromosome : CHR 3: 369,933,03-369,858,65
Locus : 3p22.2
Alt. Genes : SERF2
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