Apolipoprotein A-I
| Pathway Name | Organism |
|---|---|
| ABC transporters in lipid homeostasis | Homo sapiens |
| Amyloid fiber formation | Homo sapiens |
| Chylomicron assembly | Homo sapiens |
| Chylomicron remodeling | Homo sapiens |
| Defective ABCA1 causes TGD | Homo sapiens |
| HDL assembly | Homo sapiens |
| HDL clearance | Homo sapiens |
| HDL remodeling | Homo sapiens |
| Heme signaling | Homo sapiens |
| PPARA activates gene expression | Homo sapiens |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | |
| DOID:0080958 | primary hypoalphalipoproteinemia 2 | |
| DOID:10652 | Alzheimer's disease | |
| DOID:13810 | familial hypercholesterolemia | |
| DOID:1387 | hypolipoproteinemia | |
| DOID:1936 | atherosclerosis | |
| DOID:5844 | myocardial infarction | |
| DOID:9074 | systemic lupus erythematosus |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: August 4, 2025