This gene encodes a protein that contains olfactomedin-like and collagen-like domains. The encoded protein, which exists in both transmembrane and secreted forms, promotes formation of the nodes of Ranvier in the peripheral nervous system. Mutations in this gene cause a form of lethal congenital contracture syndrome in human patients. Autoantibodies to the encoded protein have been identified in sera form patients with multifocal motor neuropathy. [provided by RefSeq, May 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| GLDN-20-RE | 20 (40 μL) | 200 μL |  |
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| GLDN-20-OR | 20 (40 μL) | 200 μL |  |
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| GLDN-20-GO | 20 (40 μL) | 200 μL |  |
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| GLDN-20-GR | 20 (40 μL) | 200 μL |  |
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| GLDN-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein that contains olfactomedin-like and collagen-like domains. The encoded protein, which exists in both transmembrane and secreted forms, promotes formation of the nodes of Ranvier in the peripheral nervous system. Mutations in this gene cause a form of lethal congenital contracture syndrome in human patients. Autoantibodies to the encoded protein have been identified in sera form patients with multifocal motor neuropathy. [provided by RefSeq, May 2017]
Gene Symbol : GLDN
Gene Name : Gliomedin
Chromosome : CHR 15: 513,415,15-514,133,64
Locus : 15q21.2
Alt. Genes : PREB
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