Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CCNQ-20-RE | 20 (40 μL) | 200 μL |  |
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| CCNQ-20-OR | 20 (40 μL) | 200 μL |  |
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| CCNQ-20-GO | 20 (40 μL) | 200 μL |  |
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| CCNQ-20-GR | 20 (40 μL) | 200 μL |  |
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| CCNQ-20-AQ | 20 (40 μL) | 200 μL |  |
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Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]
Gene Symbol : CCNQ
Gene Name : Cyclin Q
Chromosome : CHR X: 153,599,176-153,587,924
Locus : Xq28
Alt. Genes : AKAP9
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