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)

which is involved in cellular growth

An important paralog of C1R is HP

The encoded protein is primarily composed of 22 spectrin repeats which are involved in dimer formation

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.