SLC24A5 and oculocutaneous albinism: It is a well-known gene in the pigment cell arena and is associated with a new form of OCA, named as OCA6 (MIM 609802). SLC24A5 gene was located in the chromosomal position of 15q21.1 [11]. SLC24A5 mutations were detected in patients of diverse ethnic origins, thus indicating that OCA6 is not restricted to the Chinese population.