RecName: Full=Ankyrin repeat domain-containing protein 31

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Pathogenic variants of meiotic double strand break (DSB) formation genes PRDM9 and ANKRD31 in premature ovarian insufficiency. [Genet Med. 2021]
Pathogenic variants of meiotic double strand break (DSB) formation genes PRDM9 and ANKRD31 in premature ovarian insufficiency.
Wang Y, Guo T, Ke H, Zhang Q, Li S, Luo W, Qin Y. Genet Med. 2021 Dec; 23(12):2309-2315. Epub 2021 Jul 13.
Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype. [Hum Genet. 2016]
Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype.
Lucariello M, Vidal E, Vidal S, Saez M, Roa L, Huertas D, Pineda M, Dalfó E, Dopazo J, Jurado P, et al. Hum Genet. 2016 Dec; 135(12):1343-1354. Epub 2016 Aug 19.
REC114 Partner ANKRD31 Controls Number, Timing, and Location of Meiotic DNA Breaks. [Mol Cell. 2019]
REC114 Partner ANKRD31 Controls Number, Timing, and Location of Meiotic DNA Breaks.
Boekhout M, Karasu ME, Wang J, Acquaviva L, Pratto F, Brick K, Eng DY, Xu J, Camerini-Otero RD, Patel DJ, et al. Mol Cell. 2019 Jun 6; 74(5):1053-1068.e8. Epub 2019 Apr 16.

RefSeq genomic sequence
See the genomic reference sequence for the ANKRD31 gene (NG_053151.1).
RefSeq protein isoforms
See 28 reference sequence protein isoforms for the ANKRD31 gene.

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Q8N7Z5 [Domain Mapping of Disease Mut...]
Q8N7Z5
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein