The protein encoded by this gene belongs to the family of cytoplasmic linker proteins, which have been proposed to mediate the interaction between specific membranous organelles and microtubules. This protein was found to associate with both microtubules and an organelle called the dendritic lamellar body. This gene is hemizygously deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CLIP2-20-RE | 20 (40 μL) | 200 μL |  |
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| CLIP2-20-OR | 20 (40 μL) | 200 μL |  |
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| CLIP2-20-GO | 20 (40 μL) | 200 μL |  |
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| CLIP2-20-GR | 20 (40 μL) | 200 μL |  |
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| CLIP2-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene belongs to the family of cytoplasmic linker proteins, which have been proposed to mediate the interaction between specific membranous organelles and microtubules. This protein was found to associate with both microtubules and an organelle called the dendritic lamellar body. This gene is hemizygously deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq, Jul 2008]
Gene Symbol : CLIP2
Gene Name : CAP-Gly domain containing linker protein 2
Chromosome : CHR 7: 742,894,36-744,059,42
Locus : 7q11.23
Alt. Genes : ZNF263
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