The protein encoded by this gene is part of a protein complex that mediates degradation of inositol 1,4,5-trisphosphate receptors in the endoplasmic reticulum. The encoded protein also binds cholesterol and regulates the SREBP signaling pathway, which promotes cellular cholesterol homeostasis. Defects in this gene have been associated with spastic paraplegia 62. [provided by RefSeq, Dec 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ERLIN1-20-RE | 20 (40 μL) | 200 μL |  |
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| ERLIN1-20-OR | 20 (40 μL) | 200 μL |  |
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| ERLIN1-20-GO | 20 (40 μL) | 200 μL |  |
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| ERLIN1-20-GR | 20 (40 μL) | 200 μL |  |
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| ERLIN1-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is part of a protein complex that mediates degradation of inositol 1,4,5-trisphosphate receptors in the endoplasmic reticulum. The encoded protein also binds cholesterol and regulates the SREBP signaling pathway, which promotes cellular cholesterol homeostasis. Defects in this gene have been associated with spastic paraplegia 62. [provided by RefSeq, Dec 2016]
Gene Symbol : ERLIN1
Gene Name : ER lipid raft associated 1
Chromosome : CHR 10: 100,186,056-100,150,089
Locus : 10q24.31
Alt. Genes : CLEC3A
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