Entity Details

Primary name BAAT
Entity type gene
Source Source Link

Details

PrimaryID570
RefseqGeneNG_009774
SymbolBAAT
Namebile acid-CoA:amino acid N-acyltransferase
Chromosome9
Location9q31.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1998-07-30
ModificationDate2021-06-12

Ontological Relatives

UniProt IDsBAAT_HUMAN

GO terms

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GOName
GO:0001889 liver development
GO:0002152 bile acid conjugation
GO:0005777 peroxisome
GO:0005782 peroxisomal matrix
GO:0005829 cytosol
GO:0006544 glycine metabolic process
GO:0006631 fatty acid metabolic process
GO:0006637 acyl-CoA metabolic process
GO:0006699 bile acid biosynthetic process
GO:0008104 protein localization
GO:0008206 bile acid metabolic process
GO:0016290 palmitoyl-CoA hydrolase activity
GO:0016410 N-acyltransferase activity
GO:0019530 taurine metabolic process
GO:0031100 animal organ regeneration
GO:0033882 choloyl-CoA hydrolase activity
GO:0047617 acyl-CoA hydrolase activity
GO:0047963 glycine N-choloyltransferase activity
GO:0052689 carboxylic ester hydrolase activity
GO:0052815 medium-chain acyl-CoA hydrolase activity
GO:0052816 long-chain acyl-CoA hydrolase activity
GO:0052817 very long chain acyl-CoA hydrolase activity
GO:0102991 myristoyl-CoA hydrolase activity

Diseases

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Disease IDSourceNameDescription
607748 OMIMFamilial hypercholanemia (FHCA)A disorder characterized by elevated serum bile acid concentrations, itching, and fat malabsorption. The disease may be caused by variants affecting distinct genetic loci, including the gene represented in this entry.