CPRiL

NAA10

N-alpha-acetyltransferase 10, NatA catalytic subunit

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]

• N-alpha-acetyltransferase 10
• ARD1 homolog A, N-acetyltransferase
• N-acetyltransferase ARD1, human homolog of
N-terminal acetyltransferase complex ARD1 subunit homolog A
arrest defective protein 1
microphthalmia or anophthalmia and associated anomalies
natA catalytic subunit Naa10
ARD1
ARD1A
ARD1P
DXS707
LZMS
MAA
MCOPS1
NATD
OGDNS
TE2
hARD1