This gene encodes a protein containing a coiled-coil domain. The encoded protein functions in the regulation of NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) by interacting with COMMD (copper metabolism Murr1 domain-containing) proteins. The mouse orthologous protein has been shown to bind copines, which are calcium-dependent, membrane-binding proteins that may function in calcium signaling. This human gene has been identified as a novel candidate gene for syndromic X-linked intellectual disability. [provided by RefSeq, Aug 2013]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CCDC22-20-RE | 20 (40 μL) | 200 μL |  |
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| CCDC22-20-OR | 20 (40 μL) | 200 μL |  |
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| CCDC22-20-GO | 20 (40 μL) | 200 μL |  |
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| CCDC22-20-GR | 20 (40 μL) | 200 μL |  |
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| CCDC22-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein containing a coiled-coil domain. The encoded protein functions in the regulation of NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) by interacting with COMMD (copper metabolism Murr1 domain-containing) proteins. The mouse orthologous protein has been shown to bind copines, which are calcium-dependent, membrane-binding proteins that may function in calcium signaling. This human gene has been identified as a novel candidate gene for syndromic X-linked intellectual disability. [provided by RefSeq, Aug 2013]
Gene Symbol : CCDC22
Gene Name : Coiled-coil domain containing 22
Chromosome : CHR X: 492,354,66-492,505,25
Locus : Xp11.23
Alt. Genes : FAM13A
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