bile acid-CoA:amino acid N-acyltransferase
| UniProt | Protein Name |
|---|---|
| Q14032 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| liver development | ||
| bile acid conjugation | ||
| glycine metabolic process | ||
| fatty acid metabolic process | ||
| acyl-CoA metabolic process |
| GO Term | Evidence Code | PMID |
|---|---|---|
| peroxisome | ||
| peroxisome | ||
| peroxisomal matrix | ||
| cytosol | ||
| cytosol |
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| N-acyltransferase activity | ||
| acyltransferase activity | ||
| choloyl-CoA hydrolase activity | ||
| acyl-CoA hydrolase activity |
| Gene Ontology |
|---|
| acyl-CoA metabolic process |
| fatty acid metabolic process |
| thiolester hydrolase activity |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0014667 | disease of metabolism |
| 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 |
|
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 101036806 | SAIBB32774 | ||
| 101096116 | FELCA29172 | ||
| 101572569 | OCTDE15570 | ||
| 101608698 | JACJA08396 | ||
| 101671389 | MUSPF15541 | ||
| 101716142 | HETGA27672 | ||
| 101974093 | ICTTR00673 | ||
| 102009387 | CHILA06646 | ||
| 102009722 | CHILA06646 | ||
| 102132073 | MACFA11578 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: August 4, 2025