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Gene: NAA10 (N(alpha)-acetyltransferase 10, NatA catalytic subunit) Homo sapiens
Symbol: NAA10
Name: N(alpha)-acetyltransferase 10, NatA catalytic subunit
Description: 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]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: ARD1; ARD1 homolog A, N-acetyltransferase; ARD1 homolog, N-acetyltransferase; ard1 homolog, n-acetyltransferase (s. cerevisiae); ARD1A; ARD1P; DXS707; FLJ78896; hARD1; MAA; MCOPS1; MGC71248; microphthalmia or anophthalmia and associated anomalies; N-acetyltransferase ARD1, human homolog of; N-alpha-acetyltransferase 10; N-alpha-acetyltransferase 10, NatA catalytic subunit; N-terminal acetyltransferase complex ARD1 subunit homolog A; natA catalytic subunit; natA catalytic subunit Naa10; NATD; OGDNS; TE2
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Human AssemblyChrPosition (strand)SourceGenome Browsers
GRCh38X153,929,827 - 153,935,154 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X153,195,280 - 153,200,607 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X152,848,571 - 152,853,662 (-)NCBINCBI36hg18NCBI36
Build 34X152,716,223 - 152,721,315NCBI
CeleraX153,429,094 - 153,434,185 (-)NCBI
Cytogenetic MapXq28NCBI
HuRefX141,847,939 - 141,853,239 (-)NCBIHuRef
CHM1_1X153,069,735 - 153,075,062 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)

Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Phenotype Annotations
References - curated
References - uncurated


Comparative Map Data
Position Markers
miRNA Target Status


Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
More on NAA10
Alliance Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1349422
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-07-09
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.