Homo sapiens cDNA FLJ44410 fis, clone TUTER2002729, moderately similar - 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 alternative splicing
See 25 reference mRNA sequence splice variants for the M1AP gene.

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Nucleotide