This gene is one of several genes identified in a region of the X chromosome associated with an X-linked cleft palate (CPX) disorder. The encoded protein contains a motif similar to a motif found in zinc-finger proteins. Mutation analysis of this gene has not revealed any mutation which causes the CPX disorder. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2011]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CPXCR1-20-RE | 20 (40 μL) | 200 μL |  |
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| CPXCR1-20-OR | 20 (40 μL) | 200 μL |  |
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| CPXCR1-20-GO | 20 (40 μL) | 200 μL |  |
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| CPXCR1-20-GR | 20 (40 μL) | 200 μL |  |
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| CPXCR1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is one of several genes identified in a region of the X chromosome associated with an X-linked cleft palate (CPX) disorder. The encoded protein contains a motif similar to a motif found in zinc-finger proteins. Mutation analysis of this gene has not revealed any mutation which causes the CPX disorder. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Sep 2011]
Gene Symbol : CPXCR1
Gene Name : CPX chromosome region, candidate 1
Chromosome : CHR X: 887,472,24-887,547,84
Locus : Xq21.31
Alt. Genes : SRRM1
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