NAA10

Name

N-alpha-acetyltransferase 10, NatA catalytic subunit

Type

protein-coding

Chromosome

X

Position

153,928,799–153,935,083 (−)

Aliases

ARD1, ARD1A, ARD1P, DXS707, LZMS, MAA, MCOPS1, NATD, OGDNS, TE2

Ensembl

ENSG00000102030

RefSeq RNA

NM_001256119.2, NM_001256120.2, NM_003491.4

RefSeq protein

NP_001243048.1, NP_001243049.1, NP_003482.1

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].

via MyGene.info

Gene · Ensembl

N-alpha-acetyltransferase 10, NatA catalytic subunit

Symbol

NAA10

Biotype

Protein coding

Organism

Homo sapiens

Location

Chr X:153,928,799-153,935,083

Strand

Reverse (−)

Assembly

GRCh38

Wikidata facts

Instance of

gene

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