{"symbol":"FKBP6","synonyms":["FKBP36"],"name":"FK506 binding protein 6, 36kDa","description":"The protein encoded by this gene is a cis-trans peptidyl-prolyl isomerase that may function in immunoregulation and basic cellular processes involving protein folding and trafficking. This gene is located in a chromosomal region that is deleted in Williams-Beuren syndrome. Defects in this gene may cause male infertility. There are multiple pseudogenes for this gene located nearby on chromosome 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]","ncbiEntrezGeneId":8468,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/8468","proteins":[{"symbol":"FKBP6_HUMAN","href":"/api/1.0/protein/FKBP6_HUMAN"}],"hgncRootFamilies":[{"name":"Peptidylprolyl isomerases","href":"/api/1.0/gene_family/Peptidylprolyl+isomerases"}]}