abnormal brain ependyma motile cilium physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of the tiny, motile hair-like projections from the epithelial cells that line the ventricles in the brain, which beat in concert and to move cerebrospinal fluid (Mammalian Phenotype Ontology, MP_0011069)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011069
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Genes

5 gene mutations causing the abnormal brain ependyma motile cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARL6 ADP-ribosylation factor-like 6
DNAAF2 dynein, axonemal, assembly factor 2
DYX1C1 dyslexia susceptibility 1 candidate 1
EFHC1 EF-hand domain (C-terminal) containing 1
HYDIN HYDIN, axonemal central pair apparatus protein