{"symbol":"IFT43","synonyms":["SRTD18","RP81","CED3","C14ORF179"],"name":"intraflagellar transport 43","description":"This gene encodes a subunit of the intraflagellar transport complex A (IFT-A). IFT-A is a multiprotein complex that plays an important role in cilia assembly and maintenance by mediating retrograde ciliary transport. Mutations in this gene are a cause of cranioectodermal dysplasia-3 (CED3), also known as Sensenbrenner syndrome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]","ncbiEntrezGeneId":112752,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/112752","proteins":[{"symbol":"IFT43_HUMAN","href":"/api/1.0/protein/IFT43_HUMAN"}],"hgncRootFamilies":[{"name":"Intraflagellar transport proteins (IFT)","href":"/api/1.0/gene_family/Intraflagellar+transport+proteins+%28IFT%29"}]}