{"symbol":"LCA5","synonyms":["C6ORF152"],"name":"Leber congenital amaurosis 5","description":"This gene encodes a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Alternatively spliced transcript variants are described. [provided by RefSeq, Oct 2009]","ncbiEntrezGeneId":167691,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/167691","proteins":[{"symbol":"LCA5_HUMAN","href":"/api/1.0/protein/LCA5_HUMAN"}],"hgncRootFamilies":[]}