CEP68 Polyclonal Antibody, 100ul Pipette Controller A mutation in this gene

A mutation in this gene has been associated with bilateral nasolacrimal duct obstruction (LCDD)

The protein encoded by this gene is a subunit of a bipartite UDP-N-acetylglucosamine transferase

which are thought to be involved in protein-protein interactions

however| the expression pattern suggests a role in lipid homeostasis in cells of the immune system

Because of high levels in the urine of male domestic cats| this enzyme is also called cauxin (carboxylesterase-like urinary excreted protein)

CEP68 Polyclonal Antibody, 100ul Pipette Controller A mutation in this geneCEP68 (Centrosomal Protein 68) is a Protein Coding gene. Diseases associated with CEP68 include Retinitis Pigmentosa 28. Involved in maintenance of centrosome cohesion, probably as part of a linker structure which prevents centrosome splitting (PubMed: 18042621). Required for localization of CDK5RAP2 to the centrosome during interphase.