WDR62 Rabbit Polyclonal Antibody, 20ul Cell Dissociation mutations in this gene and

mutations in this gene and the BBS8 gene are thought to play a minor role and mutations in chaperonin-like BBS genes are found to be a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population

iscellaneous: the gorilla and orangutan orthologous proteins do not exist

CKS1B protein binds to the catalytic subunit of the cyclin dependent kinases and is essential for their biological function

and macular dystrophy syndrome (EEMS)

platelet dense granules

WDR62 Rabbit Polyclonal Antibody, 20ul Cell Dissociation mutations in this gene andThis gene is proposed to play a role in cerebral cortical development. Mutations in this gene have been associated with microencephaly cortical malformations and mental retardation. Alternative splicing results in multiple transcript variants.