This gene encodes a ubiquitously expressed protein of unknown function. It has high levels of mRNA expression in the brain, heart, and retina and the protein co-localizes with polyglutamylated tubulin at the base of the primary cilium in human retinal pigment epithelial cells. Mutations in this gene have been associated with autosomal recessive cone-rod dystrophy (arCRD) and retinitis pigmentosa (arRP). [provided by RefSeq, Mar 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| C8ORF37-20-RE | 20 (40 μL) | 200 μL |  |
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| C8ORF37-20-OR | 20 (40 μL) | 200 μL |  |
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| C8ORF37-20-GO | 20 (40 μL) | 200 μL |  |
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| C8ORF37-20-GR | 20 (40 μL) | 200 μL |  |
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| C8ORF37-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a ubiquitously expressed protein of unknown function. It has high levels of mRNA expression in the brain, heart, and retina and the protein co-localizes with polyglutamylated tubulin at the base of the primary cilium in human retinal pigment epithelial cells. Mutations in this gene have been associated with autosomal recessive cone-rod dystrophy (arCRD) and retinitis pigmentosa (arRP). [provided by RefSeq, Mar 2012]
Gene Symbol : C8ORF37
Gene Name : Chromosome 8 open reading frame 37
Chromosome : CHR 8: 952,706,01-952,449,12
Locus : 8q22.1
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