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Immunogen sequence: MIQLTATPV SALVDEPVHI QATGLIPFQM VSFQASLEDE NGDMFYSQAH YRANEFGEVD LNHASSLGGD YMGVHPMGLF WSLKPEKLLT RLLKRDVMNR PFQVQVKLYD LELIVNNKVA SAPKASLTLE RWYVAPGVTR IKVREGRLRG ALFLPPGEGL FPGVIDLFGG LGGLLEFRAS LLASRGFASL ALAYHNYEDL PRKPEVTDLE YFEEAANFLL RHPKVFGSGV GVVSVCQGVQ IGLSMAIYLK QVTATVLING TNFPFGIPQV YHGQIHQPLP HSAQLISTNA LGLLELYRTF ETTQVGASQY LFPIEEAQGQ FLFIVGEGDK TINSKAHAEQ AIGQLKRHGK NNWTLLSYPG AGHLIEPPYS PLCCASTTHD LRLHWGGEVI PHAAAQEHAW KEIQRFLRKH LIPDVTSQL (1-418 aa encoded by BC009567 )
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.
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Protein Aliases: BACAT; bile acid CoA: amino acid N-acyltransferase (glycine N-choloyltransferase); bile acid CoA:amino acid N-acyltransferase; bile acid Coenzyme A: amino acid N-acyltransferase (glycine N-choloyltransferase); Bile acid-CoA thioesterase; Bile acid-CoA:amino acid N-acyltransferase; bile acid-Coenzyme A dehydrogenase: amino acid n-acyltransferase; Choloyl-CoA hydrolase; Glycine N-choloyltransferase; Long-chain fatty-acyl-CoA hydrolase; taurine N-acyltransferase
Gene Aliases: AI118337; AI158864; BAAT; BACAT; BAT
UniProt ID: (Human) Q96L31, (Mouse) Q91X34
Entrez Gene ID: (Human) 570, (Mouse) 12012
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