CEP41, centrosomal protein 41

CEP41, centrosomal protein 41

• This gene encodes a centrosomal and microtubule-binding protein which is predicted to have two coiled-coil domains and a rhodanese domain. In human retinal pigment epithelial cells the protein localized to centrioles and cilia. Mutations in this gene have been associated with Joubert Syndrome 15; an autosomal recessive ciliopathy and neurological disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]

• Gene Synonyms (JBTS15, TSGA14, centrosomal protein of 41 kDa, centrosomal protein 41 kDa, centrosomal protein 41kDa, testis specific protein A14, testis specific, 14, testis-specific gene A14 protein,)
• NCBI Gene ID: 95681
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q9BYV8
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

centrosomal protein 41 interacts with:

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