2. Gene
  3. NAA15 - N-alpha-acetyltransferase 15, NatA auxiliary subunit Gene

NAA15 - N-alpha-acetyltransferase 15, NatA auxiliary subunit Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as Ga19; NATH; TBDN; MRD50; NARG1; NAT1P; TBDN100

Gene ID: 80155 | Gene type: protein coding

About NAA15

Cytogenetic location: 4q31.1 Genomic coordinates (GRCh38): 4:139,301,505-139,391,384 (from NCBI)

This gene has 15 transcripts (splice variants), 273 orthologues, 2 paralogues and is associated with 2 phenotypes. Ubiquitous expression in testis (RPKM 10.4), lymph node (RPKM 9.1) and 25 other tissues.

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 the auxillary subunit of the N-terminal acetyltransferase A (NatA) complex. [provided by RefSeq, Jan 2017]

NAA15 Products(2)

mRNA Protein Name
NM_001410842.1 NP_001397771.1 N-alpha-acetyltransferase 15, NatA auxiliary subunit isoform 2
NM_057175.5 NP_476516.1 N-alpha-acetyltransferase 15, NatA auxiliary subunit isoform 1

NAA15 Protein Structure

TPR_2

TPR_2: Tetratricopeptide repeat (82 - 113)

NARP1

NARP1: NMDA receptor-regulated protein 1 (187 - 698)

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  • 866 a.a.
Protein Preferred Names Protein Names

N-alpha-acetyltransferase 15, NatA auxiliary subunit

N-terminal acetyltransferase

Related Diseases

Diseases Alias
Intellectual Developmental Disorder, Autosomal Dominant 50, With Behavioral Abnormalities

Mental Retardation, Autosomal Dominant 50

MRD50

Autosomal Dominant Intellectual Developmental Disorder 50

Autosomal Dominant Intellectual Developmental Disorder-50 With Behavioral Abnormalities

Autosomal Dominant Mental Retardation 50
Autism

Autistic Disorder

Autism Susceptibility 1

Childhood Autism

Autistic Disorder Of Childhood Onset

Infantile Autism

Kanner'S Syndrome

Autistic
Ogden Syndrome

OGDNS

N-Terminal Acetyltransferase Deficiency

NATD

N-Alpha-Acetyltransferase

X-Linked Malformation And Infantile Lethality Syndrome

Premature Aging Appearance-Developmental Delay-Cardiac Arrhythmia Syndrome
Microphthalmia, Syndromic 1

MCOPS1

Lenz Microphthalmia Syndrome

Lenz Dysplasia

Mcops4

Syndromic Microphthalmia 1

Lenz Microphthalmia

Maa

Microphthalmia Or Anophthalmos With Associated Anomalies

Syndromic Microphthalmia Type 4

Microphthalmia, Syndromic 4

Microphthalmia, Syndromic 4, Formerly

Mcops4, Formerly

Anop1, Formerly

Maa, Formerly

Lenz Type Microphthalmia

Syndromic Microphthalmia 4

Microphthalmia Lenz Type

Microphthalmia Syndromic 1

Syndromic Microphthalmia Type 1

Microphthalmia Syndromic 4

Microphthalmia With Ankyloblepharon And Intellectual Disability

Microphthalmia, Lenz Type

Microphthalmia-Ankyloblepharon-Intellectual Disability Syndrome

Microphthalmia, Syndromic, 1

Anop1

Microphthalmia, Syndromic, Type 1
Intellectual Developmental Disorder, Autosomal Dominant 10

MRD10

Mental Retardation, Autosomal Dominant 10

Autosomal Dominant Non-Syndromic Intellectual Disability 10

Autosomal Dominant Intellectual Developmental Disorder 10

Autosomal Dominant Mental Retardation 10

Mental Retardation, Autosomal Dominant, Type 10
Microcephaly And Chorioretinopathy 2
Syndromic Microphthalmia

Microphthalmia, Syndromic
Gastric Cancer

Stomach Cancer

Gastric Carcinoma

Stomach Carcinoma

Gastric Cancer, Somatic

Gastric Neoplasm

Carcinoma Of Stomach

Stomach Neoplasms

Malignant Neoplasm Of Stomach

Gastric Cancer Risk After H. Pylori Infection

Cancer Of The Stomach

Adult Stomach Cancer

Adult Stomach Carcinoma

GASC

Gastric Cancer Intestinal

Gastric Cancers

Gastric Carcinomas

Cancer, Gastric

Stomach Neoplasm

Malignant Neoplasm Of Body Of Stomach

Malignant Tumor Of Lesser Curve Of Stomach

Gastrocarcinoma Of Unspecified Site

Leather Bottle Stomach

Carcinoma Of Fundus Of Stomach

Cancer Of Fundus Of Stomach

Primary Malignant Neoplasm Of Body Of Stomach

Cancer Of Body Of Stomach

Primary Malignant Neoplasm Of Pyloric Antrum

Pyloric Antrum Cancer

Malignant Tumour Of Stomach
Uterine Corpus Endometrial Carcinoma
Smith-Mccort Dysplasia 1

Smith-Mccort Dysplasia

SMC1

Smc

Smith Mccort Dysplasia

Smith-Mccort Dwarfism
Autism Spectrum Disorder

Asd

Autism Spectrum Disorders

Autistic Continuum

Pervasive Developmental Disorder

Pervasive Development Disorder

Autistic Behavior

Autistic Disorder

Autistic

Autistic Disorder Of Childhood Onset

Infantile Autism

Childhood Autism

Kanner Syndrome

Pervasive Developmental Delay Nos

Pervasive Developmental Disorder, Not Otherwise Specified
Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS08986 NAA15 Human Pre-designed siRNA Set A / Unkown

Orthologs Information

Species Symbol Source ID
Felis catus NAA15 VGNC VGNC:78529
Bos taurus NAA15 VGNC VGNC:53913
Rattus norvegicus NAA15 RGD RGD:1310984
Macaca mulatta NAA15 VGNC VGNC:96715
Canis familiaris NAA15 VGNC VGNC:54810
Mus musculus NAA15 MGD MGI:1922088