| Gene Symbol | CFAP298 |
| Entrez Gene ID | 56683 |
| Full Name | chromosome 21 open reading frame 59 |
| Synonyms | C21orf48,CILD26,FBB18,Kur |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | 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]. |
| Disorder MIM: | |
| Disorder Html: | Ciliary dyskinesia, primary, 26, 615500 (3) |









































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