This gene encodes a small protein that has no known functional domains. Mutations in this gene are a cause of X-linked deafness-4, and the encoded protein may play a role in the maintenance of inner ear cells subjected to mechanical stress. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2011]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SMPX-20-RE | 20 (40 μL) | 200 μL |  |
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| SMPX-20-OR | 20 (40 μL) | 200 μL |  |
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| SMPX-20-GO | 20 (40 μL) | 200 μL |  |
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| SMPX-20-GR | 20 (40 μL) | 200 μL |  |
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| SMPX-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a small protein that has no known functional domains. Mutations in this gene are a cause of X-linked deafness-4, and the encoded protein may play a role in the maintenance of inner ear cells subjected to mechanical stress. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2011]
Gene Symbol : SMPX
Gene Name : Small muscle protein, X-linked
Chromosome : CHR X: 217,581,59-217,059,71
Locus : Xp22.12
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