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 |
---|---|---|
phosphatidylcholine-sterol O-acyltransferase activity | ||
sterol esterase activity | ||
platelet-activating factor acetyltransferase activity | ||
apolipoprotein A-I binding | ||
protein binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:2355 | anemia | |
DOID:2361 | macrocytic anemia | |
DOID:2394 | ovarian cancer | |
DOID:2477 | motor peripheral neuropathy | |
DOID:2527 | nephrosis | |
DOID:2565 | macular corneal dystrophy | |
DOID:2566 | corneal dystrophy | |
DOID:2590 | familial nephrotic syndrome | |
DOID:2717 | Bloom syndrome | |
DOID:2921 | glomerulonephritis |
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 |
---|---|---|---|
113445308 | PSETE18151 | ||
100073500 | ORNAN27636 | ||
100916426 | SARHA03186 | ||
108587667 | CALJA21642 | ||
102126888 | MACFA25176 | ||
701872 | MACMU25819 | ||
105491393 | MACNE07777 | ||
100126664 | PAPAN15586 | ||
105551486 | MANLE34900 | ||
109023671 | GORGO12122 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024