Homo sapiens meiosis specific with OB-fold (MEIOB), transcript variant - Nucleotide

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Novel MEIOB pathogenic variants including a homozygous non-canonical splicing variant, cause meiotic arrest and human non-obstructive azoospermia. [Clin Genet. 2024]
Novel MEIOB pathogenic variants including a homozygous non-canonical splicing variant, cause meiotic arrest and human non-obstructive azoospermia.
Zhu X, Hu K, Cheng H, Wu H, Li K, Gao Y, Lv M, Xu C, Geng H, Shen Q, et al. Clin Genet. 2024 Jan; 105(1):99-105. Epub 2023 Sep 16.
Nuclear localization of human MEIOB requires its NLS in the OB domain and interaction with SPATA22. [Acta Biochim Biophys Sin (Shan...]
Nuclear localization of human MEIOB requires its NLS in the OB domain and interaction with SPATA22.
Xu Y, Chen Z, Wu P, Qu W, Shi H, Cheng M, Xu Y, Jin T, Liu C, Li Y, et al. Acta Biochim Biophys Sin (Shanghai). 2022 Nov 25; 55(1):154-161.
Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia. [Front Genet. 2022]
Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia.
Wang Y, Liu L, Tan C, Meng G, Meng L, Nie H, Du J, Lu GX, Lin G, He WB, et al. Front Genet. 2022; 13:936264. Epub 2022 Aug 5.

RefSeq protein product
See the reference protein sequence for meiosis-specific with OB domain-containing protein isoform 2 (NP_689977.2).

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Protein sequence from Nucleotide coding region
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Nucleotide