CEP41 Gene

centrosomal protein 41kDa

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]

CEP41 Gene Set

From Hub Proteins Protein-Protein Interactions

interacting proteins for hub protein CEP41 from the curated Hub Proteins Protein-Protein Interactions dataset.

CEP41 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for CEP41 from the Pathway Commons Protein-Protein Interactions dataset.