This gene encodes a centrosomal and microtubule-binding protein which is predicted to have two coiled-coil domains and a rhodanese domain. In human retinal pigment epithelial cells the protein localized to centrioles and cilia. Mutations in this gene have been associated with Joubert Syndrome 15; an autosomal recessive ciliopathy and neurological disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CEP41-20-RE | 20 (40 μL) | 200 μL |  |
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| CEP41-20-OR | 20 (40 μL) | 200 μL |  |
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| CEP41-20-GO | 20 (40 μL) | 200 μL |  |
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| CEP41-20-GR | 20 (40 μL) | 200 μL |  |
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| CEP41-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a centrosomal and microtubule-binding protein which is predicted to have two coiled-coil domains and a rhodanese domain. In human retinal pigment epithelial cells the protein localized to centrioles and cilia. Mutations in this gene have been associated with Joubert Syndrome 15; an autosomal recessive ciliopathy and neurological disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]
Gene Symbol : CEP41
Gene Name : Centrosomal protein 41
Chromosome : CHR 7: 130,441,209-130,393,770
Locus : 7q32.2
Alt. Genes : FEM1B
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