Homo sapiens N-acetyltransferase 15 (GCN5-related, putative), mRNA (cD - Nucleotide

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Biallelic NAA60 variants with impaired n-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications. [Nat Commun. 2024]
Biallelic NAA60 variants with impaired n-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications.
Chelban V, Aksnes H, Maroofian R, LaMonica LC, Seabra L, Siggervåg A, Devic P, Shamseldin HE, Vandrovcova J, Murphy D, et al. Nat Commun. 2024 Mar 13; 15(1):2269. Epub 2024 Mar 13.
NAA60 (HAT4): the newly discovered bi-functional Golgi member of the acetyltransferase family. [Clin Epigenetics. 2022]
NAA60 (HAT4): the newly discovered bi-functional Golgi member of the acetyltransferase family.
Donnarumma F, Tucci V, Ambrosino C, Altucci L, Carafa V. Clin Epigenetics. 2022 Dec 21; 14(1):182. Epub 2022 Dec 21.
Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains. [Cell Rep. 2020]
Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains.
Haenig C, Atias N, Taylor AK, Mazza A, Schaefer MH, Russ J, Riechers SP, Jain S, Coughlin M, Fontaine JF, et al. Cell Rep. 2020 Aug 18; 32(7):108050.

RefSeq alternative splicing
See 9 reference mRNA sequence splice variants for the NAA60 gene.

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Nucleotide