Ceruloplasmin
| GO Term |
|---|
| extracellular region |
| extracellular space |
| plasma membrane |
| endoplasmic reticulum lumen |
| lysosomal membrane |
| extracellular exosome |
| blood microparticle |
| GO Term |
|---|
| iron ion transport |
| intracellular iron ion homeostasis |
| intracellular copper ion homeostasis |
| Pathway Name | Organism |
|---|---|
| Defective CP causes aceruloplasminemia (ACERULOP) | Homo sapiens |
| Defective SLC40A1 causes hemochromatosis 4 (HFE4) (macrophages) | Homo sapiens |
| Iron uptake and transport | Homo sapiens |
| Metal ion SLC transporters | Homo sapiens |
| Post-translational protein phosphorylation | Homo sapiens |
| Regulation of IGF Activity by IGFBP | Homo sapiens |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050711 | aceruloplasminemia | |
| DOID:12119 | hemosiderosis | |
| DOID:1826 | epilepsy |
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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