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:0111369 | hyperalphalipoproteinemia 1 | |
DOID:10127 | cerebral artery occlusion | |
DOID:10138 | xerophthalmia | |
DOID:10140 | dry eye syndrome | |
DOID:10230 | aortic atherosclerosis | |
DOID:10595 | Charcot-Marie-Tooth disease | |
DOID:10652 | Alzheimer's disease | |
DOID:1074 | kidney failure | |
DOID:10923 | sickle cell anemia | |
DOID:10952 | nephritis |
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 |
---|---|---|---|
24530 | RGD:2993 | RATNO14838 | |
100727686 | CAVPO10940 | ||
101592481 | OCTDE03539 | ||
101700977 | HETGA10387 | ||
100021772 | MONDO04952 | ||
103673641 | URSMA21373 | ||
113876702 | BOBOX12786 | ||
100941922 | OTOGA03882 | ||
101068878 | TAKRU51255 | ||
102017239 | CHILA18767 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024