dynein assembly factor with WD repeat domains 1 isoform c [Mus musculu - Protein

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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.
Assessment of ciliary phenotype in primary ciliary dyskinesia by micro-optical coherence tomography. [JCI Insight. 2017]
Assessment of ciliary phenotype in primary ciliary dyskinesia by micro-optical coherence tomography.
Solomon GM, Francis R, Chu KK, Birket SE, Gabriel G, Trombley JE, Lemke KL, Klena N, Turner B, Tearney GJ, et al. JCI Insight. 2017 Mar 9; 2(5):e91702. Epub 2017 Mar 9.
Global genetic analysis in mice unveils central role for cilia in congenital heart disease. [Nature. 2015]
Global genetic analysis in mice unveils central role for cilia in congenital heart disease.
Li Y, Klena NT, Gabriel GC, Liu X, Kim AJ, Lemke K, Chen Y, Chatterjee B, Devine W, Damerla RR, et al. Nature. 2015 May 28; 521(7553):520-4. Epub 2015 Mar 25.

RefSeq mRNA
See reference mRNA sequence for the Daw1 gene (NM_001372244.1).
RefSeq protein isoforms
See 7 reference sequence protein isoforms for the Daw1 gene.

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Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource

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Protein