NAA10
From SNPedia
| is a | gene |
| is | mentioned by |
| ClinVar | NAA10 |
| GeneCards | NAA10 |
| Diseases | NAA10 |
| wikipedia | NAA10 |
| NAA10 | |
| gopubmed | NAA10 |
| EVS | NAA10 |
| HEFalMp | NAA10 |
| MyGene2 | NAA10 |
| 23andMe | NAA10 |
| # SNPs | 12 |
| Max Magnitude | Chromosome position | Summary | |
|---|---|---|---|
| rs1057518018 | 0 | 153,932,318 | |
| rs1057518605 | 0 | 153,930,794 | |
| rs1057519448 | 0 | 153,932,549 | |
| rs1557501 | 0 | 153,931,677 | |
| rs387906701 | 0 | 153,934,388 | |
| rs587776457 | 0 | 153,930,761 | |
| rs587780562 | 0 | 153,932,338 | |
| rs587780563 | 0 | 153,932,111 | |
| rs797044868 | 0 | 153,932,410 | |
| rs863225427 | 0 | 153,933,994 | |
| rs878853263 | 0 | 153,932,073 | |
| rs878853264 | 0 | 153,932,075 |
Located on the X chromosome, the NAA10 gene encodes N-alpha-acetyltransferase 10, one of the proteins in the N-alpha-acetyltransferase complex responsible for alpha-acetylation of proteins and peptides.Wikipedia
Mutations in the NAA10 gene have been associated with Ogden syndrome, an X-linked recessive disorder of infancy that can be lethal, as well as with Lenz microphthalmia syndrome.
De novo mutations in the NAA15 gene, which encodes a dimeric binding partner protein to NAA10, may have clinical consequences including intellectual disability, delayed speech and motor milestones, and autism spectrum disorder.10.1016/j.ajhg.2018.03.004
