UniProt | Protein Name |
---|---|
P04180 |
|
A0A140VK24 |
|
GO Term | Evidence Code | PMID |
---|---|---|
very-low-density lipoprotein particle remodeling | ||
phospholipid metabolic process |
GO Term | Evidence Code | PMID |
---|---|---|
high-density lipoprotein particle | ||
extracellular region |
|
|
extracellular space | ||
extracellular exosome |
GO Term | Evidence Code | PMID |
---|---|---|
1-alkyl-2-acetylglycerophosphocholine esterase activity |
DO ID | Disease Name | Source |
---|---|---|
DOID:557 | kidney disease | |
DOID:0014667 | disease of metabolism | |
DOID:0050539 | Charcot-Marie-Tooth disease type 2 | |
DOID:0050766 | choreaacanthocytosis | |
DOID:0060224 | atrial fibrillation | |
DOID:0060262 | gallbladder disease | |
DOID:0060357 | chylomicron retention disease | |
DOID:0060600 | obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum | |
DOID:0060843 | hereditary neuropathy with liability to pressure palsies | |
DOID:0070161 | hereditary sensory and autonomic neuropathy type 2 |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000083 | Renal insufficiency |
HP:0000093 | Proteinuria |
HP:0000505 | Visual impairment |
HP:0001084 | Corneal arcus |
HP:0001681 | Angina pectoris |
HP:0001744 | Splenomegaly |
HP:0001878 | Hemolytic anemia |
HP:0001895 | Normochromic anemia |
HP:0002155 | Hypertriglyceridemia |
Disease ID | Disease Name |
---|---|
ORPHA:79292 |
|
OMIM:245900 |
|
OMIM:136120 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
109050579 | CYPCA139095 | ||
103738876 | NANGA22354 | ||
116450074 | CORMO01975 | ||
103268200 | CARSF09815 | ||
115601148 | STRHB07618 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024