This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Mar 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| B9D1-20-RE | 20 (40 μL) | 200 μL |  |
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| B9D1-20-OR | 20 (40 μL) | 200 μL |  |
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| B9D1-20-GO | 20 (40 μL) | 200 μL |  |
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| B9D1-20-GR | 20 (40 μL) | 200 μL |  |
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| B9D1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Mar 2016]
Gene Symbol : B9D1
Gene Name : B9 domain containing 1
Chromosome : CHR 17: 193,781,92-193,353,71
Locus : 17p11.2
Alt. Genes : ARL4C
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