[5][6] Also known as Cep126, the protein has been shown to localize to the centrosome.

Furthermore, it is found at pericentriolar satellites and the base of the primary cilium.

Depleting Cep126 leads to dispersion of pericentriolar satellites, in turn disrupting microtubule organization at the mitotic spindle.

[7] Mutations in this gene have been found to cause monomelic amyotrophy.

This article on a gene on human chromosome 11 is a stub.