This gene encodes a protein that is thought to be involved with centrosome function. Mutations in this gene have been associated with primary microcephaly (MCPH4). Alternative splicing results in multiple transcript variants.CEP152 (Centrosomal Protein 152) is a Protein Coding gene. Diseases associated with CEP152 include Microcephaly 9, Primary, Autosomal Recessive and Seckel Syndrome 5. Among its related pathways are Regulation of PLK1 Activity at G2/M Transition and Organelle biogenesis and maintenance. GO annotations related to this gene include protein kinase binding.