cilia- and flagella-associated protein 221 isoform X5 [Homo sapiens]

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Identification of genetic variants in CFAP221 as a cause of primary ciliary dyskinesia. [J Hum Genet. 2020]
Identification of genetic variants in CFAP221 as a cause of primary ciliary dyskinesia.
Bustamante-Marin XM, Shapiro A, Sears PR, Charng WL, Conrad DF, Leigh MW, Knowles MR, Ostrowski LE, Zariwala MA. J Hum Genet. 2020 Jan; 65(2):175-180. Epub 2019 Oct 21.
The Pcdp1 complex coordinates the activity of dynein isoforms to produce wild-type ciliary motility. [Mol Biol Cell. 2011]
The Pcdp1 complex coordinates the activity of dynein isoforms to produce wild-type ciliary motility.
DiPetrillo CG, Smith EF. Mol Biol Cell. 2011 Dec; 22(23):4527-38. Epub 2011 Oct 12.
Strain-dependent brain defects in mouse models of primary ciliary dyskinesia with mutations in Pcdp1 and Spef2. [Neuroscience. 2014]
Strain-dependent brain defects in mouse models of primary ciliary dyskinesia with mutations in Pcdp1 and Spef2.
Finn R, Evans CC, Lee L. Neuroscience. 2014 Sep 26; 277:552-67. Epub 2014 Jul 27.

RefSeq mRNA
See reference mRNA sequence for the CFAP221 gene (XM_017003559.2).
RefSeq protein isoforms
See 19 reference sequence protein isoforms for the CFAP221 gene.

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Protein