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:0060580 | Noonan syndrome 2 | |
DOID:0060581 | Noonan syndrome 3 | |
DOID:0060582 | Noonan syndrome 4 | |
DOID:0060583 | Noonan syndrome 5 | |
DOID:0060584 | Noonan syndrome 6 | |
DOID:0060585 | Noonan syndrome 7 | |
DOID:0060586 | Noonan syndrome 8 | |
DOID:0060587 | Noonan syndrome 9 | |
DOID:0060588 | Noonan syndrome 10 | |
DOID:0060608 | microcephalic osteodysplastic primordial dwarfism type I |
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 |
---|---|---|---|
172309 | WB:WBGene00020258 | ||
172725 | WB:WBGene00007857 | ||
187017 | WB:WBGene00019404 | ||
189157 | WB:WBGene00020989 | ||
102356569 | LATCH00753 | ||
102363365 | LATCH03004 | ||
108707337 | Xenbase:XB-GENE-17333935 | ||
100125079 | Xenbase:XB-GENE-5872601 | ||
100924464 | SARHA12241 | ||
105593023 | CERAT33259 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024