This gene encodes a coiled-coil and calcium binding domain protein that appears to play a critical role in cilia formation. Mutations in this gene cause Meckel syndrome type 6, as well as Joubert syndrome type 9. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CC2D2A-20-RE | 20 (40 μL) | 200 μL |  |
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| CC2D2A-20-OR | 20 (40 μL) | 200 μL |  |
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| CC2D2A-20-GO | 20 (40 μL) | 200 μL |  |
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| CC2D2A-20-GR | 20 (40 μL) | 200 μL |  |
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| CC2D2A-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a coiled-coil and calcium binding domain protein that appears to play a critical role in cilia formation. Mutations in this gene cause Meckel syndrome type 6, as well as Joubert syndrome type 9. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
Gene Symbol : CC2D2A
Gene Name : Coiled-coil and C2 domain containing 2A
Chromosome : CHR 4: 154,686,59-156,019,70
Locus : 4p15.32
Alt. Genes : LRPPRC
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