Aliases for CEP97 Gene
External Ids for CEP97 Gene
Previous HGNC Symbols for CEP97 Gene
Previous GeneCards Identifiers for CEP97 Gene
GeneCards Summary for CEP97 Gene
CEP97 (Centrosomal Protein 97) is a Protein Coding gene. Diseases associated with CEP97 include Spinocerebellar Ataxia 11 and Townes-Brocks Syndrome. Among its related pathways are Organelle biogenesis and maintenance and Regulation of PLK1 Activity at G2/M Transition. Gene Ontology (GO) annotations related to this gene include calmodulin binding.
UniProtKB/Swiss-Prot for CEP97 Gene
Acts as a key negative regulator of ciliogenesis in collaboration with CCP110 by capping the mother centriole thereby preventing cilia formation. Required for recruitment of CCP110 to the centrosome.