The protein encoded by this gene is similar to that of KIP/CIB, calcineurin B, and calmodulin. The encoded protein is a calcium-binding regulatory protein that interacts with DNA-dependent protein kinase catalytic subunits (DNA-PKcs), and it is involved in photoreceptor cell maintenance. Mutations in this gene cause deafness, autosomal recessive, 48 (DFNB48), and also Usher syndrome 1J (USH1J). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CIB2-20-RE | 20 (40 μL) | 200 μL |  |
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| CIB2-20-OR | 20 (40 μL) | 200 μL |  |
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| CIB2-20-GO | 20 (40 μL) | 200 μL |  |
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| CIB2-20-GR | 20 (40 μL) | 200 μL |  |
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| CIB2-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is similar to that of KIP/CIB, calcineurin B, and calmodulin. The encoded protein is a calcium-binding regulatory protein that interacts with DNA-dependent protein kinase catalytic subunits (DNA-PKcs), and it is involved in photoreceptor cell maintenance. Mutations in this gene cause deafness, autosomal recessive, 48 (DFNB48), and also Usher syndrome 1J (USH1J). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]
Gene Symbol : CIB2
Gene Name : Calcium and integrin binding family member 2
Chromosome : CHR 15: 781,319,75-781,046,05
Locus : 15q25.1
Alt. Genes : ZNF263
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