This gene encodes a protein which regulates Golgi-associated secretory pathways that are essential to endochondral bone formation during early development. This gene is also believed to play a role in early brain development. This gene is widely expressed in embryos and is particularly abundant in chodrocytes and brain tissues. It encodes a peripheral membrane protein which shuttles between the cytosol and Golgi complex. Mutations in this gene are associated with two types of recessive osteochondrodysplasia: Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia. [provided by RefSeq, Jun 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| DYM-20-RE | 20 (40 μL) | 200 μL |  |
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| DYM-20-OR | 20 (40 μL) | 200 μL |  |
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| DYM-20-GO | 20 (40 μL) | 200 μL |  |
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| DYM-20-GR | 20 (40 μL) | 200 μL |  |
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| DYM-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein which regulates Golgi-associated secretory pathways that are essential to endochondral bone formation during early development. This gene is also believed to play a role in early brain development. This gene is widely expressed in embryos and is particularly abundant in chodrocytes and brain tissues. It encodes a peripheral membrane protein which shuttles between the cytosol and Golgi complex. Mutations in this gene are associated with two types of recessive osteochondrodysplasia: Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia. [provided by RefSeq, Jun 2017]
Gene Symbol : DYM
Gene Name : Dymeclin
Chromosome : CHR 18: 494,607,08-490,414,73
Locus : 18q21.1
Alt. Genes : ZNF263
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