Homo sapiens meiosis 1 associated protein (M1AP), transcript variant 1 - Nucleotide

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Structural analysis of M1AP variants associated with severely impaired spermatogenesis causing male infertility. [PeerJ. 2022]
Structural analysis of M1AP variants associated with severely impaired spermatogenesis causing male infertility.
Gerlevik U, Ergoren MC, Sezerman OU, Temel SG. PeerJ. 2022; 10:e12947. Epub 2022 Mar 21.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome. [Cell. 2021]
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, et al. Cell. 2021 May 27; 184(11):3022-3040.e28. Epub 2021 May 6.
Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility. [Am J Hum Genet. 2020]
Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility.
Wyrwoll MJ, Temel ŞG, Nagirnaja L, Oud MS, Lopes AM, van der Heijden GW, Heald JS, Rotte N, Wistuba J, Wöste M, et al. Am J Hum Genet. 2020 Aug 6; 107(2):342-351. Epub 2020 Jul 15.

RefSeq protein product
See the reference protein sequence for meiosis 1 arrest protein isoform 1 (NP_620159.2).

Protein
Protein sequence from Nucleotide coding region
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Homo sapiens meiosis 1 associated protein (M1AP), transcript variant 1, mRNA
Homo sapiens meiosis 1 associated protein (M1AP), transcript variant 1, mRNA
gi|1890333660|ref|NM_138804.5|

Nucleotide

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Nucleotide