PREDICTED: Homo sapiens cilia and flagella associated protein 221 (CFA - Nucleotide

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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.
Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease. [Respir Res. 2014]
Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease.
Lee JH, Cho MH, Hersh CP, McDonald ML, Crapo JD, Bakke PS, Gulsvik A, Comellas AP, Wendt CH, Lomas DA, et al. Respir Res. 2014 Sep 21; 15(1):113. Epub 2014 Sep 21.
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 alternative splicing
See 19 reference mRNA sequence splice variants for the CFAP221 gene.
RefSeq protein product
See the reference protein sequence for cilia- and flagella-associated protein 221 isoform X1 (XP_016859040.1).