Coagulation factor XII
| GO Term | Evidence Code | Reference |
|---|---|---|
| plasma kallikrein-kinin cascade | ||
| plasma kallikrein-kinin cascade | ||
| Factor XII activation | ||
| blood coagulation | ||
| blood coagulation, intrinsic pathway |
| GO Term | Evidence Code | Reference |
|---|---|---|
| extracellular region | ||
| extracellular region | ||
| extracellular region | ||
| obsolete extracellular space |
|
|
| rough endoplasmic reticulum |
| GO Term | Evidence Code | Reference |
|---|---|---|
| serine-type endopeptidase activity | ||
| serine-type endopeptidase activity | ||
| serine-type endopeptidase activity | ||
| serine-type endopeptidase activity | ||
| serine-type endopeptidase activity |
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 43 |
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| 109 |
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| 181 |
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| 249 |
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| 285 |
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| 299 |
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| 305 |
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| 308 |
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| 311 |
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| 328 |
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| Pathway Name | Organism |
|---|---|
| Defective SERPING1 causes hereditary angioedema | Homo sapiens |
| Defective factor XII causes hereditary angioedema | Homo sapiens |
| Intrinsic Pathway of Fibrin Clot Formation | Homo sapiens |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080940 | hereditary angioedema type III | |
| DOID:14735 | hereditary angioedema | |
| DOID:1558 | angioedema | |
| DOID:2231 | factor XII deficiency | |
| DOID:224 | transient cerebral ischemia | |
| DOID:3525 | middle cerebral artery infarction | |
| DOID:5844 | myocardial infarction |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: April 6, 2026