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Gene : BAAT Homo sapiens

Name  ? bile acid-CoA:amino acid N-acyltransferase Cytological Location  9q31.1
Brief Description  bile acid-CoA:amino acid N-acyltransferase
description  The protein encoded by this gene is a liver enzyme that catalyzes the transfer of C24 bile acids from the acyl-CoA thioester to either glycine or taurine, the second step in the formation of bile acid-amino acid conjugates. The bile acid conjugates then act as a detergent in the gastrointestinal tract, which enhances lipid and fat-soluble vitamin absorption. Defects in this gene are a cause of familial hypercholanemia (FHCA). Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]
  • synonyms:
  • BAT,
  • uc010mtd.3,
  • bile acid Coenzyme A:amino acid N-acyltransferase (glycine N-choloyltransferase),
  • NM_001701,
  • bile acid CoA: amino acid N-acyltransferase (glycine N-choloyltransferase),
  • L34081,
  • OTTHUMG00000020377,
  • BAAT,
  • HGNC:932,
  • BACAT,
  • BAT,
  • glycine N-choloyltransferase
  • identifiers:
  • 570,
  • ENSG00000136881,
  • BAAT

Genome feature

Region: gene ? Length: 24589  
Location: 9:101360417-101385005 reverse strand Cyto location: 9q31.1


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1 Diseases

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577 SN Ps

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19 Data Sets

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0 Located Features

90 Rna Seq Results