RecName: Full=Bromodomain and WD repeat-containing protein 1; AltName: - Protein

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Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia. [Hum Genet. 2021]
Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia.
Guo T, Tu CF, Yang DH, Ding SZ, Lei C, Wang RC, Liu L, Kang X, Shen XQ, Yang YF, et al. Hum Genet. 2021 May; 140(5):761-773. Epub 2021 Jan 3.
BRWD1 orchestrates epigenetic landscape of late B lymphopoiesis. [Nat Commun. 2018]
BRWD1 orchestrates epigenetic landscape of late B lymphopoiesis.
Mandal M, Maienschein-Cline M, Maffucci P, Veselits M, Kennedy DE, McLean KC, Okoreeh MK, Karki S, Cunningham-Rundles C, Clark MR. Nat Commun. 2018 Sep 24; 9(1):3888. Epub 2018 Sep 24.
Mouse BRWD1 is critical for spermatid postmeiotic transcription and female meiotic chromosome stability. [J Cell Biol. 2015]
Mouse BRWD1 is critical for spermatid postmeiotic transcription and female meiotic chromosome stability.
Pattabiraman S, Baumann C, Guisado D, Eppig JJ, Schimenti JC, De La Fuente R. J Cell Biol. 2015 Jan 5; 208(1):53-69. Epub 2014 Dec 29.

RefSeq genomic sequence
See the genomic reference sequence for the BRWD1 gene (NG_029919.3).
RefSeq protein isoforms
See 14 reference sequence protein isoforms for the BRWD1 gene.

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Q9NSI6 [Domain Mapping of Disease Mut...]
Q9NSI6
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
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Protein