C21orf59( Human )

Entrez Gene 56683 Entrez Gene 56683
chromosome 21 open reading frame 59

Alias

C21orf48|CILD26|FBB18|Kur

This gene encodes a protein that plays a critical role in dynein arm assembly and motile cilia function. Mutations in this gene result in primary ciliary dyskinesia. Naturally occuring readthrough transcription occurs from this locus to the downstream t-complex 10 like (TCP10L) gene. [provided by RefSeq, Apr 2017].

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