The protein encoded by this gene localizes to the basal body and is required for formation of the primary cilium in ciliated epithelial cells. Mutations in this gene result in Meckel syndrome type 1 and in Bardet-Biedl syndrome type 13. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| MKS1-20-RE | 20 (40 μL) | 200 μL |  |
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| MKS1-20-OR | 20 (40 μL) | 200 μL |  |
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| MKS1-20-GO | 20 (40 μL) | 200 μL |  |
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| MKS1-20-GR | 20 (40 μL) | 200 μL |  |
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| MKS1-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene localizes to the basal body and is required for formation of the primary cilium in ciliated epithelial cells. Mutations in this gene result in Meckel syndrome type 1 and in Bardet-Biedl syndrome type 13. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]
Gene Symbol : MKS1
Gene Name : Meckel syndrome, type 1
Chromosome : CHR 17: 582,196,04-582,054,35
Locus : 17q22
Alt. Genes : DNAL4
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