Homo sapiens dynein assembly factor with WD repeats 1 (DAW1), transcri - Nucleotide

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Biallelic DAW1 variants cause a motile ciliopathy characterized by laterality defects and subtle ciliary beating abnormalities. [Genet Med. 2022]
Biallelic DAW1 variants cause a motile ciliopathy characterized by laterality defects and subtle ciliary beating abnormalities.
Leslie JS, Hjeij R, Vivante A, Bearce EA, Dyer L, Wang J, Rawlins L, Kennedy J, Ubeyratna N, Fasham J, et al. Genet Med. 2022 Nov; 24(11):2249-2261. Epub 2022 Sep 8.
Daw1 regulates the timely onset of cilia motility during development. [Development. 2022]
Daw1 regulates the timely onset of cilia motility during development.
Bearce EA, Irons ZH, Craig SB, Kuhns CJ, Sabazali C, Farnsworth DR, Miller AC, Grimes DT. Development. 2022 Jun 15; 149(12). Epub 2022 Jun 16.
Purification and crystal structure of human ODA16: Implications for ciliary import of outer dynein arms by the intraflagellar transport machinery. [Protein Sci. 2020]
Purification and crystal structure of human ODA16: Implications for ciliary import of outer dynein arms by the intraflagellar transport machinery.
Wang J, Taschner M, Petriman NA, Andersen MB, Basquin J, Bhogaraju S, Vetter M, Wachter S, Lorentzen A, Lorentzen E. Protein Sci. 2020 Jun; 29(6):1502-1510. Epub 2020 Apr 20.

RefSeq alternative splicing
See 5 reference mRNA sequence splice variants for the DAW1 gene.
RefSeq protein product
See the reference protein sequence for dynein assembly factor with WD repeat domains 1 isoform 1 (NP_849143.1).

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Protein sequence from Nucleotide coding region
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Nucleotide