abnormal 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 and the central canal of the spinal cord, which beat in concert and to move cerebrospinal fluid around the central nervous system (Mammalian Phenotype Ontology, MP_0011068)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011068
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Genes

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

Symbol Name
ARL6 ADP-ribosylation factor-like 6
CLUAP1 clusterin associated protein 1
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