Baat Gene Search Result

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18 records found for search term Baat

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RGD ID	Symbol	Name	Description	Chr	Start	Stop	Species	Annotations	Match	Type
2190	Baat	bile acid CoA:amino acid N-acyltransferase	ENCODES a protein that exhibits glycine N-choloyltransferase activity; long-chain fatty acyl-CoA hydrolase activity (ortholog); medium-chain fatty acyl-CoA hydrolase activity (ortholog); INVOLVED IN animal organ regeneration; bile acid conjugation; liver development; PARTICIPATES IN bile acid biosyn ... (more) thetic pathway; cerebrotendinous xanthomatosis pathway; congenital bile acid synthesis defect pathway; ASSOCIATED WITH Sepsis; atypical hemolytic-uremic syndrome (ortholog); disease of metabolism (ortholog); FOUND IN cytosol; peroxisome; INTERACTS WITH (+)-schisandrin B; 17beta-estradiol; 2,3,7,8-tetrachlorodibenzodioxine	5	68647166	68656137	Rat	235	symbol , PhenoGen	gene, protein-coding, PROVISIONAL [RefSeq]
10225	Baat	bile acid-Coenzyme A: amino acid N-acyltransferase	Enables N-acyltransferase activity. Acts upstream of or within bile acid metabolic process. Located in cytosol. Human ortholog(s) of this gene implicated in disease of metabolism. Orthologous to human BAAT (bile acid-CoA:amino acid N-acyltransferase). [provided ... (more) by Alliance of Genome Resources, Jul 2025]	4	49489416	49507915	Mouse	240	symbol , PhenoGen , description	gene, protein-coding, VALIDATED [RefSeq]
735913	BAAT	bile acid-CoA:amino acid N-acyltransferase	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 tra ... (more) ct, 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]	9	101360417	101385006	Human	251	symbol , COSMIC , Human Proteome Map	gene, protein-coding, REVIEWED [RefSeq]
8735738	Baat	bile acid-CoA:amino acid N-acyltransferase	ENCODES a protein that exhibits glycine N-choloyltransferase activity (ortholog); long-chain fatty acyl-CoA hydrolase activity (ortholog); medium-chain fatty acyl-CoA hydrolase activity (ortholog); INVOLVED IN acyl-CoA metabolic process (ortholog); animal organ regeneration (ortholog); bile acid bio ... (more) synthetic process (ortholog); PARTICIPATES IN bile acid biosynthetic pathway; cerebrotendinous xanthomatosis pathway; congenital bile acid synthesis defect pathway; ASSOCIATED WITH atypical hemolytic-uremic syndrome (ortholog); disease of metabolism (ortholog); Familial Hypercholanemia (ortholog); FOUND IN cytosol (ortholog); peroxisome (ortholog)	NW_004955419	24469213	24521728	Chinchilla	39	symbol	gene, protein-coding, MODEL [RefSeq]
11735356	BAAT	bile acid-CoA:amino acid N-acyltransferase	ENCODES a protein that exhibits carboxylic ester hydrolase activity (inferred); fatty acyl-CoA hydrolase activity (inferred); glycine N-choloyltransferase activity (inferred); INVOLVED IN animal organ regeneration (ortholog); bile acid metabolic process (ortholog); liver development (ortholog); PART ... (more) ICIPATES IN bile acid biosynthetic pathway; cerebrotendinous xanthomatosis pathway; congenital bile acid synthesis defect pathway; ASSOCIATED WITH atypical hemolytic-uremic syndrome (ortholog); disease of metabolism (ortholog); Familial Hypercholanemia (ortholog); FOUND IN peroxisome (ortholog)	9	72568002	72593179	Bonobo	43	symbol	gene, protein-coding, MODEL [RefSeq]
12191553	BAAT	bile acid-CoA:amino acid N-acyltransferase	ENCODES a protein that exhibits glycine N-choloyltransferase activity (inferred); long-chain fatty acyl-CoA hydrolase activity (inferred); medium-chain fatty acyl-CoA hydrolase activity (inferred); INVOLVED IN animal organ regeneration (ortholog); bile acid metabolic process (ortholog); liver develo ... (more) pment (ortholog); PARTICIPATES IN bile acid biosynthetic pathway; cerebrotendinous xanthomatosis pathway; congenital bile acid synthesis defect pathway; ASSOCIATED WITH atypical hemolytic-uremic syndrome (ortholog); disease of metabolism (ortholog); Familial Hypercholanemia (ortholog); FOUND IN peroxisome (ortholog)	11	58102057	58116750	Dog	37	symbol	gene, protein-coding, MODEL [RefSeq]
12565396	Baat	bile acid-CoA:amino acid N-acyltransferase	ENCODES a protein that exhibits fatty acyl-CoA hydrolase activity (inferred); glycine N-choloyltransferase activity (inferred); long-chain fatty acyl-CoA hydrolase activity (inferred); INVOLVED IN animal organ regeneration (ortholog); bile acid metabolic process (ortholog); liver development (orthol ... (more) og); PARTICIPATES IN bile acid biosynthetic pathway; cerebrotendinous xanthomatosis pathway; congenital bile acid synthesis defect pathway; ASSOCIATED WITH atypical hemolytic-uremic syndrome (ortholog); disease of metabolism (ortholog); Familial Hypercholanemia (ortholog); FOUND IN peroxisome (ortholog)	NW_004936524	9536032	9544901	Squirrel	38	symbol	gene, protein-coding, MODEL [RefSeq]
18339698	BAAT	bile acid-CoA:amino acid N-acyltransferase	ENCODES a protein that exhibits carboxylic ester hydrolase activity (inferred); fatty acyl-CoA hydrolase activity (inferred); glycine N-choloyltransferase activity (inferred); INVOLVED IN animal organ regeneration (ortholog); bile acid metabolic process (ortholog); liver development (ortholog); PART ... (more) ICIPATES IN bile acid biosynthetic pathway; cerebrotendinous xanthomatosis pathway; congenital bile acid synthesis defect pathway; ASSOCIATED WITH atypical hemolytic-uremic syndrome (ortholog); disease of metabolism (ortholog); Familial Hypercholanemia (ortholog); FOUND IN peroxisome (ortholog)				Green Monkey	42	symbol	gene, protein-coding, MODEL [RefSeq]
155237012	baat						Tropical Clawed Frog		symbol	gene, null
14211784	BAAT	bile acid-CoA:amino acid N-acyltransferase	ENCODES a protein that exhibits glycine N-choloyltransferase activity (inferred); long-chain fatty acyl-CoA hydrolase activity (inferred); medium-chain fatty acyl-CoA hydrolase activity (inferred); INVOLVED IN acyl-CoA metabolic process (inferred); bile acid biosynthetic process (inferred); bile aci ... (more) d conjugation (inferred); PARTICIPATES IN bile acid biosynthetic pathway; cerebrotendinous xanthomatosis pathway; congenital bile acid synthesis defect pathway; ASSOCIATED WITH atypical hemolytic-uremic syndrome (ortholog); disease of metabolism (ortholog); Familial Hypercholanemia (ortholog); FOUND IN cytosol (inferred); peroxisome (inferred)				Pig	32	symbol	gene, protein-coding, MODEL [RefSeq]
155237013	baat.S						African Clawed Frog		symbol	gene, null
14274277	LOC100515185	acyl-coenzyme A amino acid N-acyltransferase 2	ENCODES a protein that exhibits thiolester hydrolase activity (inferred); INVOLVED IN acyl-CoA metabolic process (inferred); fatty acid metabolic process (inferred)				Pig	7	old_gene_symbol	gene, protein-coding, MODEL [RefSeq]
18919314	LOC101716142	bile acid-CoA:amino acid N-acyltransferase	ENCODES a protein that exhibits acyltransferase activity (inferred); fatty acyl-CoA hydrolase activity (inferred); thiolester hydrolase activity (inferred); INVOLVED IN acyl-CoA metabolic process (inferred); fatty acid metabolic process (inferred); lipid metabolic process (inferred); FOUND IN peroxi ... (more) some (inferred)				Naked Mole-Rat	10	old_gene_symbol	gene, protein-coding, MODEL [RefSeq]
12274894	LOC481634	bile acid-CoA:amino acid N-acyltransferase	ENCODES a protein that exhibits thiolester hydrolase activity (inferred); INVOLVED IN acyl-CoA metabolic process (inferred); fatty acid metabolic process (inferred)	11	58084951	58103188	Dog	7	old_gene_symbol	gene, protein-coding, MODEL [RefSeq]
8984553	LOC102009387	bile acid-CoA:amino acid N-acyltransferase-like		NW_004955419	24443222	24466306	Chinchilla		ensembl_gene_symbol	gene, protein-coding, MODEL [RefSeq]
1318809	BRAT1	BRCA1 associated ATM activator 1	The protein encoded by this ubiquitously expressed gene interacts with the tumor suppressing BRCA1 (breast cancer 1) protein and and the ATM (ataxia telangiectasia mutated) protein. ATM is thought to be a master controller of cell cycle checkpoint signalling pathways that are required for cellular r ... (more) esponses to DNA damage such as double-strand breaks that are induced by ionizing radiation and complexes with BRCA1 in the multi-protein complex BASC (BRAC1-associated genome surveillance complex). The protein encoded by this gene is thought to play a role in the DNA damage pathway regulated by BRCA1 and ATM. [provided by RefSeq, Mar 2012]	7	2537810	2555524	Human	237	old_gene_symbol	gene, protein-coding, REVIEWED [RefSeq]
1318810	Brat1	BRCA1-associated ATM activator 1	A similar gene in human encodes a Breast Cancer 1 (BRCA1) interacting protein that is involved in cell cycle checkpoint signaling. The similar human protein is localized to DNA double strand breaks caused by ionizing radiation, and regulates cellular DNA damage response through interactions with Ata ... (more) xia Telangiectasia Mutated (ATM) and DNA-dependent Protein Kinase. A pseudogene of this gene is located on chromosome 3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]	5	140688222	140705134	Mouse	114	old_gene_symbol	gene, protein-coding, REVIEWED [RefSeq]
4144528	ACNATP	acyl-CoA:amino acid N-acyltransferase, pseudogene	INTERACTS WITH aflatoxin B1; benzo[a]pyrene; O-methyleugenol	9	101334092	101339347	Human	3	old_gene_symbol	gene, pseudo, INFERRED [RefSeq]