UniProt | Protein Name |
---|---|
Q14032 |
|
GO Term | Evidence Code | PMID |
---|---|---|
animal organ regeneration | ||
fatty acid metabolic process | ||
taurine metabolic process | ||
glycine metabolic process | ||
acyl-CoA metabolic process |
GO Term | Evidence Code | PMID |
---|---|---|
intracellular membrane-bounded organelle | ||
cytosol | ||
peroxisome | ||
peroxisomal matrix |
|
GO Term | Evidence Code | PMID |
---|---|---|
acyl-CoA hydrolase activity | ||
N-acyltransferase activity | ||
glycine N-choloyltransferase activity | ||
acyltransferase activity |
|
|
protein binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:0110345 | osteogenesis imperfecta type 16 | |
DOID:0110346 | osteogenesis imperfecta type 10 | |
DOID:0110347 | osteogenesis imperfecta type 15 | |
DOID:0110348 | osteogenesis imperfecta type 12 | |
DOID:0110349 | osteogenesis imperfecta type 9 | |
DOID:0110350 | osteogenesis imperfecta type 6 | |
DOID:0110351 | osteogenesis imperfecta type 11 | |
DOID:0110741 | type 1 diabetes mellitus 2 | |
DOID:0110742 | type 1 diabetes mellitus 3 | |
DOID:0110743 | type 1 diabetes mellitus 4 |
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 |
---|---|---|---|
105805407 | PROCO17473 | ||
103256777 | CARSF14937 |
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Last updated: August 19, 2024