EFHD1 Polyclonal Antibody, 100ul Mammalian Expression introns and silent nucleotide positions

introns and silent nucleotide positions in codons

This gene encodes a member of the mucin family of proteins

Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency

and dilated cardiomyopathy type 1X (CMD1X)

a putative neurotransmitter

EFHD1 Polyclonal Antibody, 100ul Mammalian Expression introns and silent nucleotide positionsThis 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