The specific function of this gene has yet to be determined in humans; however, in rodents, it is necessary for survival of the forebrain mesenchyme and may also be involved in development of the cervix. Mutations in the mouse gene lead to neural tube defects such as acrania and meroanencephaly. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ALX1-20-RE | 20 (40 μL) | 200 μL |  |
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| ALX1-20-OR | 20 (40 μL) | 200 μL |  |
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| ALX1-20-GO | 20 (40 μL) | 200 μL |  |
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| ALX1-20-GR | 20 (40 μL) | 200 μL |  |
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| ALX1-20-AQ | 20 (40 μL) | 200 μL |  |
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The specific function of this gene has yet to be determined in humans; however, in rodents, it is necessary for survival of the forebrain mesenchyme and may also be involved in development of the cervix. Mutations in the mouse gene lead to neural tube defects such as acrania and meroanencephaly. [provided by RefSeq, Jul 2008]
Gene Symbol : ALX1
Gene Name : ALX homeobox 1
Chromosome : CHR 12: 852,802,57-853,017,83
Locus : 12q21.31
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