Ceruloplasmin
| GO Term | Evidence Code | Reference |
|---|---|---|
| intracellular copper ion homeostasis | ||
| intracellular iron ion homeostasis | ||
| intracellular iron ion homeostasis | ||
| intracellular iron ion homeostasis |
| GO Term | Evidence Code | Reference |
|---|---|---|
| extracellular region | ||
| extracellular region | ||
| extracellular region | ||
| extracellular region | ||
| extracellular region |
| GO Term | Evidence Code | Reference |
|---|---|---|
| ferroxidase activity | ||
| ferroxidase activity | ||
| ferroxidase activity | ||
| ferroxidase activity | ||
| ferroxidase activity |
| 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:1826 | epilepsy | |
| DOID:12119 | hemosiderosis |
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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: April 6, 2026