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CABP2 belongs to a subfamily of calcium binding proteins that share similarity to calmodulin. Additionally we are shipping and and many more products for this protein.
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Genetic defects in CABP2 cause moderate-to-severe sensorineural hearing impairment.
This gene belongs to a subfamily of calcium binding proteins that share similarity to calmodulin. Like calmodulin, these family members can likely stimulate calmodulin-dependent kinase II and the protein phosphatase calcineurin. Calcium binding proteins are an important component of calcium mediated cellular signal transduction.
calcium-binding protein 2