This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| MEOX2-20-RE | 20 (40 μL) | 200 μL |  |
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| MEOX2-20-OR | 20 (40 μL) | 200 μL |  |
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| MEOX2-20-GO | 20 (40 μL) | 200 μL |  |
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| MEOX2-20-GR | 20 (40 μL) | 200 μL |  |
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| MEOX2-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease. [provided by RefSeq, Jul 2008]
Gene Symbol : MEOX2
Gene Name : Mesenchyme homeobox 2
Chromosome : CHR 7: 156,866,82-156,112,11
Locus : 7p21.2
Alt. Genes : DNAL4
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