{"symbol":"IFT172","synonyms":["SRTD10","WIM","NPHP17","SLB","OSM-1","BBS20","RP71"],"name":"intraflagellar transport 172","description":"This gene encodes a subunit of the intraflagellar transport subcomplex IFT-B. Subcomplexes IFT-A and IFT-B are necessary for ciliary assembly and maintenance. Mutations in this gene have been associated with skeletal ciliopathies, with or without polydactyly, such as such short-rib thoracic dysplasias 1, 9 or 10. [provided by RefSeq, Mar 2014]","ncbiEntrezGeneId":26160,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/26160","proteins":[{"symbol":"IF172_HUMAN","href":"/api/1.0/protein/IF172_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"}]}