{"symbol":"IFT80","synonyms":["ATD2","SRTD2","WDR56"],"name":"intraflagellar transport 80","description":"The protein encoded by this gene is part of the intraflagellar transport complex B and is necessary for the function of motile and sensory cilia. Defects in this gene are a cause of asphyxiating thoracic dystrophy 2 (ATD2). Three transcript variants encoding two different isoforms have been found for this gene.[provided by RefSeq, Jun 2010]","ncbiEntrezGeneId":57560,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/57560","proteins":[{"symbol":"IFT80_HUMAN","href":"/api/1.0/protein/IFT80_HUMAN"}],"hgncRootFamilies":[{"name":"Intraflagellar transport proteins (IFT)","href":"/api/1.0/gene_family/Intraflagellar+transport+proteins+%28IFT%29"},{"name":"WD repeat domain containing (WDR)","href":"/api/1.0/gene_family/WD+repeat+domain+containing+%28WDR%29"}]}