Automated description from the Alliance of Genome Resources (Release 7.4.0)
Predicted to enable identical protein binding activity. Predicted to be involved in cranial skeletal system development; establishment of protein localization; and midbody abscission. Located in intercellular bridge and midbody. Is expressed in cerebral cortex ventricular layer; germ cell of testis; and ovary. Used to study Meckel syndrome. Human ortholog(s) of this gene implicated in multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly. Orthologous to human CEP55 (centrosomal protein 55).
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