absent embryonic cilia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of cilia on the cells of the embryonic node (Mammalian Phenotype Ontology, MP_0004132)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004132
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Genes

17 gene mutations causing the absent embryonic cilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
C2CD3 C2 calcium-dependent domain containing 3
CLUAP1 clusterin associated protein 1
DLL1 delta-like 1 (Drosophila)
DYNC2LI1 dynein, cytoplasmic 2, light intermediate chain 1
IFT122 intraflagellar transport 122
IFT172 intraflagellar transport 172
IFT57 intraflagellar transport 57
IFT88 intraflagellar transport 88
KIAA0586 KIAA0586
KIF3A kinesin family member 3A
KIF3B kinesin family member 3B
MBD4 methyl-CpG binding domain protein 4
TCTN1 tectonic family member 1
TCTN2 tectonic family member 2
TMEM67 transmembrane protein 67
TRAF3IP1 TNF receptor-associated factor 3 interacting protein 1
WDR35 WD repeat domain 35