NAA20 N-alpha-acetyltransferase 20, NatB catalytic subunit
Gene ID: 51126, updated on 18-Sep-2024Gene type: protein coding
Also known as: NAT3; NAT5; MRT73; NAT3P; NAT5P; dJ1002M8.1
- See all available tests in GTR for this gene
- Go to complete Gene record for NAA20
- Go to Variation Viewer for NAA20 variants
Summary
NAT5 is a component of N-acetyltransferase complex B (NatB). Human NatB performs cotranslational N(alpha)-terminal acetylation of methionine residues when they are followed by asparagine (Starheim et al., 2008 [PubMed 18570629]).[supplied by OMIM, Apr 2009]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Intellectual developmental disorder, autosomal recessive 73 | not available |
Genomic context
- Location:
- 20p11.23
- Sequence:
- Chromosome: 20; NC_000020.11 (20017290..20033655)
- Total number of exons:
- 7
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for NAA20 variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.