Identity
HGNC
LOCATION
4q31.1
LOCUSID
ALIAS
Ga19,MRD50,NARG1,NAT1P,NATH,TBDN,TBDN100
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 80155
MIM: 608000
HGNC: 30782
Ensembl: ENSG00000164134
Variants:
dbSNP: 80155
ClinVar: 80155
TCGA: ENSG00000164134
COSMIC: NAA15
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000164134 | ENST00000296543 | Q9BXJ9 |
| ENSG00000164134 | ENST00000398947 | A0A0B4J1W3 |
| ENSG00000164134 | ENST00000515576 | D6RAP7 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37130971 | 2023 | Expanding the phenotypic spectrum of NAA10-related neurodevelopmental syndrome and NAA15-related neurodevelopmental syndrome. | 14 |
| 37130971 | 2023 | Expanding the phenotypic spectrum of NAA10-related neurodevelopmental syndrome and NAA15-related neurodevelopmental syndrome. | 14 |
| 35328089 | 2022 | Possible Catch-Up Developmental Trajectories for Children with Mild Developmental Delay Caused by NAA15 Pathogenic Variants. | 5 |
| 35328089 | 2022 | Possible Catch-Up Developmental Trajectories for Children with Mild Developmental Delay Caused by NAA15 Pathogenic Variants. | 5 |
| 33103328 | 2021 | Variants in NAA15 cause pediatric hypertrophic cardiomyopathy. | 11 |
| 33557580 | 2021 | Mechanisms of Congenital Heart Disease Caused by NAA15 Haploinsufficiency. | 20 |
| 33103328 | 2021 | Variants in NAA15 cause pediatric hypertrophic cardiomyopathy. | 11 |
| 33557580 | 2021 | Mechanisms of Congenital Heart Disease Caused by NAA15 Haploinsufficiency. | 20 |
| 31155310 | 2019 | Structure and Mechanism of Acetylation by the N-Terminal Dual Enzyme NatA/Naa50 Complex. | 23 |
| 31155310 | 2019 | Structure and Mechanism of Acetylation by the N-Terminal Dual Enzyme NatA/Naa50 Complex. | 23 |
| 28990276 | 2018 | Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disability. | 20 |
| 29656860 | 2018 | Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies. | 37 |
| 29754825 | 2018 | Structure of Human NatA and Its Regulation by the Huntingtin Interacting Protein HYPK. | 37 |
| 28990276 | 2018 | Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disability. | 20 |
| 29656860 | 2018 | Truncating Variants in NAA15 Are Associated with Variable Levels of Intellectual Disability, Autism Spectrum Disorder, and Congenital Anomalies. | 37 |
Citation
Dessen P
NAA15 (N-alpha-acetyltransferase 15, NatA auxiliary subunit)
Atlas Genet Cytogenet Oncol Haematol. 2010-02-01
Online version: http://atlasgeneticsoncology.org/gene/51332/naa15-(n-alpha-acetyltransferase-15-nata-auxiliary-subunit)
