Entity Details

Primary name NAT8L
Entity type gene
Source Source Link

Details

PrimaryID339983
RefseqGeneNG_027961
SymbolNAT8L
NameN-acetyltransferase 8 like
Chromosome4
Location4p16.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2003-03-28
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsNAT8L_HUMAN

GO terms

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GOName
GO:0005737 cytoplasm
GO:0005739 mitochondrion
GO:0005759 mitochondrial matrix
GO:0008080 N-acetyltransferase activity
GO:0009066 aspartate family amino acid metabolic process
GO:0016021 integral component of membrane
GO:0017188 aspartate N-acetyltransferase activity
GO:0030867 rough endoplasmic reticulum membrane
GO:0031966 mitochondrial membrane

Diseases

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Disease IDSourceNameDescription
614063 OMIMN-acetylaspartate deficiency (NACED)A metabolic disorder resulting in truncal ataxia, marked developmental delay, seizures, and secondary microcephaly. The disease is caused by variants affecting the gene represented in this entry.

Interactions

6 interactions

InteractorPartnerSourcesPublicationsLink
NAT8LPEX19BioGRID, IntAct32296183 details
NAT8LTSPAN5BioGRID, IntAct26186194 28514442 details
NAT8LKIAA0232BioGRID, IntAct26186194 28514442 details
NAT8LFLNCBioGRID26186194 details
NAT8LFAT3BioGRID26186194 details
NAT8LHNRNPH1BioGRID26760575 details