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IFT52

Official Full Name
intraflagellar transport 52
Organism
Homo sapiens
GeneID
51098
Background
This gene encodes a conserved proline-rich protein that is a component of the intraflagellar transport-B (IFT-B) core complex. The encoded protein is essential for the integrity of the IFT-B core complex, and for biosynthesis and maintenance of cilia. Mutations in this gene are associated with ciliopathy that affects the skeleton. [provided by RefSeq, Oct 2016]
Synonyms
NGD2; NGD5; CGI-53; C20orf9;

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