abnormal motile primary cilium physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of the cilia of the mouse embryo found on the cells of the embryonic node, which generate flow of extraembryonic fluid surrounding the node in a distinct twirling motion that directs fluid flow asymmetrically across the cellular surface to affect asymmetric body plan organization (Mammalian Phenotype Ontology, MP_0008933)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008933
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8 gene mutations causing the abnormal motile primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BICC1 BicC family RNA binding protein 1
DNAH11 dynein, axonemal, heavy chain 11
FOXJ1 forkhead box J1
INVS inversin
KIF3A kinesin family member 3A
MKS1 Meckel syndrome, type 1
NOTO notochord homeobox
PIFO primary cilia formation