XB-FEAT-5910468: Difference between revisions
imported>Xenbase gene generator No edit summary |
imported>Xenbase |
||
| Line 1: | Line 1: | ||
= | =cfap298= | ||
This is the community wiki page for the gene '' | This is the community wiki page for the gene ''cfap298'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase. | ||
=nomenclature changes= | |||
02/06/2018 | |||
Human symbol has changed for genepage ID: 5910468 From c21orf59 to cfap298 | |||
Human symbol has changed for Entrez Gene: 56683. From C21orf59 to CFAP298 | |||
Human name has changed for Entrez Gene: 56683. From chromosome 21 open reading frame 59 to cilia and flagella associated protein 298 | |||
=Summary from NCBI= | |||
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] | |||
Latest revision as of 07:37, 6 February 2018
cfap298
This is the community wiki page for the gene cfap298 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
nomenclature changes
02/06/2018 Human symbol has changed for genepage ID: 5910468 From c21orf59 to cfap298
Human symbol has changed for Entrez Gene: 56683. From C21orf59 to CFAP298
Human name has changed for Entrez Gene: 56683. From chromosome 21 open reading frame 59 to cilia and flagella associated protein 298
Summary from NCBI
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]