Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
84316
Gene name Gene Name - the full gene name approved by the HGNC.
N-alpha-acetyltransferase 38, NatC auxiliary subunit
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NAA38
Synonyms (NCBI Gene) Gene synonyms aliases
LSMD1, MAK31, PFAAP2
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17p13.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT650261 hsa-miR-8063 HITS-CLIP 23824327
MIRT664992 hsa-miR-138-2-3p HITS-CLIP 23824327
MIRT650262 hsa-miR-129-5p HITS-CLIP 23824327
MIRT650261 hsa-miR-8063 HITS-CLIP 23824327
MIRT650262 hsa-miR-129-5p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003723 Function RNA binding IEA
GO:0005515 Function Protein binding IPI 19398576, 25416956, 32814053, 33961781
GO:0005634 Component Nucleus IDA 19398576
GO:0005634 Component Nucleus IEA
GO:0005654 Component Nucleoplasm IDA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
617990 28212 ENSG00000183011
Protein
UniProt ID Q9BRA0
Protein name N-alpha-acetyltransferase 38, NatC auxiliary subunit (LSM domain-containing protein 1) (Phosphonoformate immuno-associated protein 2)
Protein function Auxillary component of the N-terminal acetyltransferase C (NatC) complex which catalyzes acetylation of N-terminal methionine residues (PubMed:19398576, PubMed:37891180). N-terminal acetylation protects proteins from ubiquitination and degradati
PDB 7MX2
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01423 LSM 43 114 LSM domain Domain
Sequence
MAGAGPTMLLREENGCCSRRQSSSSAGDSDGEREDSAAERARQQLEALLNKTMRIRMTDG
RTLVGCFLCTDRDCNVILGSAQEFLKPSDSFSAGEPRVLGLAMVPGHHIVSIEV
QRESLT
GPPYL
Sequence length 125
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Asthma Asthma N/A N/A GWAS
Gout Gout N/A N/A GWAS
Hypertension Hypertension N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Associate 26474971