CEP85 Rabbit Polyclonal Antibody, 50ul miRNA / siRNA Synthesis Mutations in this gene are

Mutations in this gene are associated with Pendred syndrome

The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome

PTM:Phosphorylated by NEK2 which may regulate its association with centrosomes

which are structurally related to the major histocompatibility complex (MHC) proteins and form heterodimers with beta-2-microglobulin

including in thyroid

CEP85 Rabbit Polyclonal Antibody, 50ul miRNA / siRNA Synthesis Mutations in this gene areThis gene encodes a protein that belongs to the centrosome associated family of proteins. The centrosome is a subcellular organelle in the animal cell that functions as a microtubule organizing center and is involved in cell cycle progression. Alternate splicing results in multiple transcript variants.