RecName: Full=Zinc finger MYND domain-containing protein 11; AltName: - Protein

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ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder. [Clin Genet. 2021]
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder.
Oates S, Absoud M, Goyal S, Bayley S, Baulcomb J, Sims A, Riddett A, Allis K, Brasch-Andersen C, Balasubramanian M, et al. Clin Genet. 2021 Oct; 100(4):412-429. Epub 2021 Jul 16.
ZMYND11-related syndromic intellectual disability: 16 patients delineating and expanding the phenotypic spectrum. [Hum Mutat. 2020]
ZMYND11-related syndromic intellectual disability: 16 patients delineating and expanding the phenotypic spectrum.
Yates TM, Drucker M, Barnicoat A, Low K, Gerkes EH, Fry AE, Parker MJ, O'Driscoll M, Charles P, Cox H, et al. Hum Mutat. 2020 May; 41(5):1042-1050. Epub 2020 Mar 5.
The Transcriptional Repressor BS69 is a Conserved Target of the E1A Proteins from Several Human Adenovirus Species. [Viruses. 2018]
The Transcriptional Repressor BS69 is a Conserved Target of the E1A Proteins from Several Human Adenovirus Species.
Zhang A, Tessier TM, Galpin KJC, King CR, Gameiro SF, Anderson WW, Yousef AF, Qin WT, Li SSC, Mymryk JS. Viruses. 2018 Nov 22; 10(12). Epub 2018 Nov 22.

RefSeq genomic sequence
See the genomic reference sequence for the ZMYND11 gene (NG_029960.1).
RefSeq protein isoforms
See 38 reference sequence protein isoforms for the ZMYND11 gene.

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Q15326 [Domain Mapping of Disease Mut...]
Q15326
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
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reagents
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Protein