Automated description from the Alliance of Genome Resources (Release 9.0.0)
Predicted to contribute to protein carrier activity. Acts upstream of or within several processes, including embryonic limb morphogenesis; embryonic organ development; and myotome development. Located in motile cilium and photoreceptor connecting cilium. Part of intraciliary transport particle A. Is expressed in several structures, including alimentary system; genitourinary system; hemolymphoid system gland; liver; and lung. Used to study ciliopathy. Human ortholog(s) of this gene implicated in several diseases, including Caroli disease; asphyxiating thoracic dystrophy 5; cranioectodermal dysplasia 4; nephronophthisis 13; and spermatogenic failure 72. Orthologous to human WDR19 (WD repeat domain 19).
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