Mks

This unpublished dataset is based on the [Cc2d2a](https://www.alliancegenome.org/gene/MGI:1924487) gene, which is: involved in cilium assembly and protein localization to ciliary transition zone. Acts upstream of or within several processes, including animal organ development; cilium assembly; and neural tube closure. Located in ciliary transition zone. Part of MKS complex. Used to study Meckel syndrome and visceral heterotaxy. Human ortholog(s) of this gene implicated in Joubert syndrome 9; Meckel syndrome 6; and intellectual disability. Orthologous to human CC2D2A. The Mks (Cc2d2a) data are closely related to the other ciliopathy datasets in MusMorph, including B9d, Ift, and Tctn.