NYX Rabbit Polyclonal Antibody, 20ul Molecular Sciences Mutations in this gene are

Mutations in this gene are the cause of thrombocythemia 1

Rigorously tested for leakage

while other individuals have an allele encoding a protein that is predicted to be non-functional

Two transcript variants encoding the same protein have been identified for PARK7

The protein encoded by this gene is a major sialoglycoprotein found on the surface of thymocytes| T lymphocytes| monocytes| granulocytes| and some B lymphocytes

NYX Rabbit Polyclonal Antibody, 20ul Molecular Sciences Mutations in this gene areThe product of this gene belongs to the small leucine rich proteoglycan (SLRP) family of proteins. Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1) also called X linked congenital stationary night blindness (XLCSNB). CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision myopia hyperopia nystagmus and reduced visual acuity. The role of other SLRP proteins suggests that mutations