Gene Symbol | NAA10 |
Entrez Gene ID | 8260 |
Full Name | N(alpha)-acetyltransferase 10, NatA catalytic subunit |
Synonyms | ARD1,ARD1A,ARD1P,DXS707,MCOPS1,NATD,OGDNS,TE2,hARD1 |
General protein information |
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Gene Type | protein-coding |
Organism | Homo sapiens(human) |
Genome | |
Summary | N-alpha-acetylation is among the most common post-translational protein modifications in eukaryotic cells. This process involves the transfer of an acetyl group from acetyl-coenzyme A to the alpha-amino group on a nascent polypeptide and is essential for normal cell function. This gene encodes an N-terminal acetyltransferase that functions as the catalytic subunit of the major amino-terminal acetyltransferase A complex. Mutations in this gene are the cause of Ogden syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]. |
Disorder MIM: | |
Disorder Html: | Ogden syndrome, 300855 (3); ?Microphthalmia, syndromic 1, 309800 (3) |