{"symbol":"HYDIN","synonyms":["HYDIN1","PPP1R31","HYDIN2","CILD5"],"name":"HYDIN, axonemal central pair apparatus protein","description":"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]","ncbiEntrezGeneId":54768,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/54768","proteins":[{"symbol":"HYDIN_HUMAN","href":"/api/1.0/protein/HYDIN_HUMAN"}],"hgncRootFamilies":[{"name":"Protein phosphatase 1 regulatory subunits (PPP1R)","href":"/api/1.0/gene_family/Protein+phosphatase+1+regulatory+subunits+%28PPP1R%29"}]}