This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SMNDC1-20-RE | 20 (40 μL) | 200 μL |  |
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| SMNDC1-20-OR | 20 (40 μL) | 200 μL |  |
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| SMNDC1-20-GO | 20 (40 μL) | 200 μL |  |
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| SMNDC1-20-GR | 20 (40 μL) | 200 μL |  |
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| SMNDC1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene. [provided by RefSeq, Jul 2008]
Gene Symbol : SMNDC1
Gene Name : Survival motor neuron domain containing 1
Chromosome : CHR 10: 110,304,968-110,293,039
Locus : 10q25.2
Alt. Genes : ENAM
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