CCZ1 Polyclonal Antibody, AbBy Fluor™ 405 Conjugated

Chromosome 7 is about 158 milllion bases long, encodes over 1000 genes and makes up about 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf28 gene product has been provisionally designated C7orf28 pending further characterization.

C7orf28A; CCZ1 vacuolar protein trafficking and biogenesis associated homolog S. cerevisiae; CCZ1A; CGI-43; H_DJ1163J12.2; Vacuolar fusion protein CCZ1 homolog; CCZ1_HUMAN.