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IFT172

Official Full Name
intraflagellar transport 172
Organism
Homo sapiens
GeneID
26160
Background
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]
Synonyms
SLB; wim; RP71; BBS20; osm-1; NPHP17; SRTD10;

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