The protein encoded by this gene belongs to the ERG4/ERG24 family. It localized in the nuclear envelope inner membrane and anchors the lamina and the heterochromatin to the membrane. It may mediate interaction between chromatin and lamin B. Mutations of this gene has been associated with autosomal recessive HEM/Greenberg skeletal dysplasia. Alternative splicing occurs at this locus and two transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| LBR-20-RE | 20 (40 μL) | 200 μL |  |
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| LBR-20-OR | 20 (40 μL) | 200 μL |  |
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| LBR-20-GO | 20 (40 μL) | 200 μL |  |
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| LBR-20-GR | 20 (40 μL) | 200 μL |  |
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| LBR-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene belongs to the ERG4/ERG24 family. It localized in the nuclear envelope inner membrane and anchors the lamina and the heterochromatin to the membrane. It may mediate interaction between chromatin and lamin B. Mutations of this gene has been associated with autosomal recessive HEM/Greenberg skeletal dysplasia. Alternative splicing occurs at this locus and two transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]
Gene Symbol : LBR
Gene Name : Lamin B receptor
Chromosome : CHR 1: 225,428,854-225,401,501
Locus : 1q42.12
Alt. Genes : LRPPRC
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