HYDIN( Human )
HYDIN, axonemal central pair apparatus protein
Alias
CILD5|HYDIN1|HYDIN2|PPP1R31
This gene encodes a protein that may be involved in cilia motility. Mutations in this gene cause of autosomal recessive primary ciliary dyskinesia-5, a disorder characterized by the accumulation of cerebrospinal fluid within the ventricles of the brain. A duplicate copy of this gene has been found in humans on chromosome 1. [provided by RefSeq, Jan 2013].