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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
bile acid-CoA:amino acid N-acyltransferase
Summary
- Gene Symbol
-
- BAAT
- Aliases
-
- BAT
- glycine N-choloyltransferase
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Acyltransferase
- Cytoplasm
- Direct protein sequencing
- Disease variant
- Fatty acid metabolism
- Peroxisome
- Phosphoprotein
- Reference proteome
- Serine esterase
- Proteins
| UniProt | Protein Name |
|---|---|
| Q14032 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| bile acid metabolic process |
|
|
| bile acid biosynthetic process | ||
| liver development | ||
| taurine metabolic process |
GO Hierarchy
biological process
metabolic process [inference]
nitrogen compound metabolic process [inference]
cellular metabolic process [inference]
primary metabolic process [inference]
small molecule metabolic process [inference]
organic substance metabolic process [inference]
cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| peroxisome | ||
| intracellular membrane-bounded organelle | ||
| peroxisomal matrix |
|
|
| cytosol |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| acyltransferase activity |
|
|
| protein binding | ||
| choloyl-CoA hydrolase activity | ||
| carboxylic ester hydrolase activity | ||
| N-acyltransferase activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- acyl-coenzyme A thioesterase
- Functional Category
-
- E: Amino acid transport and metabolism
- I: Lipid transport and metabolism
- J: Translation, ribosomal structure and biogenesis
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| acyl-CoA metabolic process |
| fatty acid metabolic process |
| thiolester hydrolase activity |
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0014667 | disease of metabolism |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000952 | Jaundice |
| HP:0001399 | Hepatic failure |
| HP:0002240 | Hepatomegaly |
| HP:0002748 | Rickets |
| HP:0002908 | Conjugated hyperbilirubinemia |
| HP:0003593 | Infantile onset |
| HP:0003621 | Juvenile onset |
| HP:0011463 | Childhood onset |
| Disease ID | Disease Name |
|---|---|
| OMIM:619232 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP000423
- Gene Name
- bile acid CoA:amino acid N-acyltransferase
Ortholog
| Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 100431907 | 9601_0:002611 | PONAB36684 | ||
| 100476252 | AILME05309 | |||
| 100598200 | NOMLE18037 | |||
| 100670223 | LOXAF17277 | |||
| 100719973 | CAVPO12781 | |||
| 100756252 | CRIGR12158 | |||
| 100924464 | SARHA12241 | |||
| 100957390 | OTOGA15713 | |||
| 100992429 | 9597_0:0028b7 | PANPA39970 | ||
| 101007875 | PAPAN08606 |
