This gene encodes a transmembrane low-density lipoprotein receptor that binds and internalizes ligands in the process of receptor-mediated endocytosis. This protein also acts as a co-receptor with Frizzled protein family members for transducing signals by Wnt proteins and was originally cloned on the basis of its association with type 1 diabetes mellitus in humans. This protein plays a key role in skeletal homeostasis and many bone density related diseases are caused by mutations in this gene. Mutations in this gene also cause familial exudative vitreoretinopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| LRP5BA-20-REGO | 20 (40 μL) | 200 μL |
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| LRP5BA-20-REGR | 20 (40 μL) | 200 μL |
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| LRP5BA-20-ORGR | 20 (40 μL) | 200 μL |
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| LRP5BA-20-GOGR | 20 (40 μL) | 200 μL |
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| LRP5BA-20-GRRE | 20 (40 μL) | 200 μL |
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| LRP5BA-20-GROR | 20 (40 μL) | 200 μL |
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| LRP5BA-20-GRGO | 20 (40 μL) | 200 μL |
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| LRP5BA-20-AQOR | 20 (40 μL) | 200 μL |
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This gene encodes a transmembrane low-density lipoprotein receptor that binds and internalizes ligands in the process of receptor-mediated endocytosis. This protein also acts as a co-receptor with Frizzled protein family members for transducing signals by Wnt proteins and was originally cloned on the basis of its association with type 1 diabetes mellitus in humans. This protein plays a key role in skeletal homeostasis and many bone density related diseases are caused by mutations in this gene. Mutations in this gene also cause familial exudative vitreoretinopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]
Gene Symbol : LRP5
Gene Name : LDL receptor related protein 5
Chromosome : CHR 11: 682,988,65-684,492,74
Locus : 11q13.2
Alt. Genes : ZNF263
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