EFHD1 Polyclonal Antibody, 100ul Mammalian Expression A mutation in this gene

A mutation in this gene is associated with young-adult onset of nonsyndromic deafness-64

They are implicated in a number of cellular processes involving alteration of RNA secondary structure

introns and silent nucleotide positions in codons

and dilated cardiomyopathy type 1X (CMD1X)

EFHD1 Polyclonal Antibody, 100ul Mammalian Expression A mutation in this geneThis gene encodes a member of the EF hand super family of calcium binding proteins, which are involved in a variety of cellular processes including mitosis, synaptic transmission, and cytoskeletal rearrangement. The protein encoded by this gene is composed of an N terminal disordered region, proline rich elements, two EF hands, and a C terminal coiled coil domain. This protein has been shown to associate with the mitochondrial inner membrane, and in