1. Gene
  2. NAA30 - N-alpha-acetyltransferase 30, NatC catalytic subunit Gene

NAA30 - N-alpha-acetyltransferase 30, NatC catalytic subunit Gene

Homo sapiens

Also known as MAK3; Mak3p; NAT12; NAT12P; C14orf35

Gene ID: 122830 | Gene type: protein coding

About NAA30

Cytogenetic location: 14q22.3 Genomic coordinates (GRCh38): 14:57,390,586-57,415,906 (from NCBI)

This gene has 4 transcripts (splice variants), 213 orthologues and 4 paralogues. Ubiquitous expression in testis (RPKM 11.4), brain (RPKM 9.1) and 25 other tissues.

Summary

Enables peptide alpha-N-acetyltransferase activity. Involved in N-terminal peptidyl-methionine acetylation. Located in cytosol and nucleus. Part of NatC complex. Colocalizes with polysome. [provided by Alliance of Genome Resources, Apr 2022]

NAA30 Products(1)

mRNA Protein Name
NM_001011713.3 NP_001011713.2 N-alpha-acetyltransferase 30

NAA30 Protein Structure

Acetyltransf_1

Acetyltransf_1: Acetyltransferase (GNAT) family (261 - 338)

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  • 362 a.a.
Protein Preferred Names Protein Names

N-alpha-acetyltransferase 30

N-acetyltransferase 12 (GCN5-related, putative)

Related Diseases

Diseases Alias
Neurogenic Arthropathy

Neuropathic Arthropathy

Arthropathy Associated With Neurological Disorder

Charcot'S Arthropathy

Charcot'S Joint

Arthropathy, Neurogenic

Charcot Joint

Charcot Or Tabetic Arthropathy

Charcot Foot

Villonodular Synovitis

Pigmented Villonodular Synovitis

Ochronosis
Chondrocalcinosis

Pseudogout

Calcium Pyrophosphate Deposition Disease

Familial Chondrocalcinosis

Chondrocalcinosis Nos

Cppd - [Calcium Pyrophosphate Deposition Disease]

Cpdd - [Calcium Pyrophosphate Deposition Disease]

Chondrocalcinosis, Due To Pyrophosphate Crystals, Involving Unspecified Site

Chondrocalcinosis, Cause Unspecified

Chondrocalcinosis Due To Pyrophosphate Crystals

Chondrocalcinosis Articularis

Calcium Pyrophosphate Arthritis And Periarthritis

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

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

Orthologs Information

Species Symbol Source ID
Mus musculus NAA30 MGD MGI:1922259
Bos taurus NAA30 VGNC VGNC:54627
Rattus norvegicus NAA30 RGD RGD:1559923
Canis familiaris NAA30 VGNC VGNC:50549
Macaca mulatta NAA30 VGNC VGNC:84405
Felis catus NAA30 VGNC VGNC:80907