This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| MNX1-20-RE | 20 (40 μL) | 200 μL |  |
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| MNX1-20-OR | 20 (40 μL) | 200 μL |  |
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| MNX1-20-GO | 20 (40 μL) | 200 μL |  |
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| MNX1-20-GR | 20 (40 μL) | 200 μL |  |
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| MNX1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]
Gene Symbol : MNX1
Gene Name : Motor neuron and pancreas homeobox 1
Chromosome : CHR 7: 157,010,652-157,004,852
Locus : 7q36.3
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