This gene encodes a lysyl oxidase, which likely functions as an amine oxidase and plays a role in the formation of crosslinks in collagens and elastin. Deletion of the related gene in mouse causes neonatal mortality with cleft palate, spine deformity, and defects in collagen organization. A mutation in this gene was found in a family with Stickler syndrome. [provided by RefSeq, Sep 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| LOXL3-20-RE | 20 (40 μL) | 200 μL |  |
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| LOXL3-20-OR | 20 (40 μL) | 200 μL |  |
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| LOXL3-20-GO | 20 (40 μL) | 200 μL |  |
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| LOXL3-20-GR | 20 (40 μL) | 200 μL |  |
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| LOXL3-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a lysyl oxidase, which likely functions as an amine oxidase and plays a role in the formation of crosslinks in collagens and elastin. Deletion of the related gene in mouse causes neonatal mortality with cleft palate, spine deformity, and defects in collagen organization. A mutation in this gene was found in a family with Stickler syndrome. [provided by RefSeq, Sep 2016]
Gene Symbol : LOXL3
Gene Name : Lysyl oxidase like 3
Chromosome : CHR 2: 745,557,08-745,322,57
Locus : 2p13.1
Alt. Genes : CELA3A
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