{"symbol":"C21ORF59","synonyms":["C21ORF48","CILD26","CFAP298","FBB18","C21orf59","Kur"],"name":"chromosome 21 open reading frame 59","description":"This gene encodes a protein that plays a critical role in dynein arm assembly and motile cilia function. Mutations in this gene result in primary ciliary dyskinesia. Naturally occuring readthrough transcription occurs from this locus to the downstream t-complex 10 like (TCP10L) gene. [provided by RefSeq, Apr 2017]","ncbiEntrezGeneId":56683,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/56683","proteins":[{"symbol":"CU059_HUMAN","href":"/api/1.0/protein/CU059_HUMAN"}],"hgncRootFamilies":[]}