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MIRAGE
protein C, inactivator of coagulation factors Va and VIIIa
Summary
- Gene Symbol
-
- PROC
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Blood coagulation
- Calcium
- Cleavage on pair of basic residues
- Direct protein sequencing
- Disease variant
- Disulfide bond
- EGF-like domain
- Endoplasmic reticulum
- Gamma-carboxyglutamic acid
- Glycoprotein
- Golgi apparatus
- Hydroxylation
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Repeat
- Secreted
- Serine protease
- Signal
- Thrombophilia
- Zymogen
- Proteins
| UniProt | Protein Name |
|---|---|
| B4DPQ3 |
|
| E7END6 |
|
| P04070 |
|
| B4DPC8 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| proteolysis | ||
| blood coagulation | ||
| negative regulation of blood coagulation | ||
| negative regulation of blood coagulation | ||
| negative regulation of apoptotic process |
GO Hierarchy
biological process
biological regulation [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum lumen | ||
| Golgi apparatus | ||
| Golgi lumen |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| serine-type endopeptidase activity | ||
| serine-type endopeptidase activity | ||
| serine-type endopeptidase activity | ||
| calcium ion binding | ||
| protein binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- serine protease
- Functional Category
-
- E: Amino acid transport and metabolism
- Q: Secondary metabolites biosynthesis, transport and catabolism
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| blood coagulation |
| hydrolase activity |
| proteolysis |
| serine-type endopeptidase activity |
| serine-type peptidase activity |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060903 | thrombosis | |
| DOID:0111902 | thrombophilia due to activated protein C resistance | |
| DOID:0111904 | autosomal recessive thrombophilia due to protein C deficiency | |
| DOID:0111909 | autosomal dominant thrombophilia due to protein C deficiency | |
| DOID:10591 | pre-eclampsia | |
| DOID:14115 | toxic shock syndrome | |
| DOID:2450 | central retinal vein occlusion | |
| DOID:2452 | thrombophilia | |
| DOID:2841 | asthma | |
| DOID:2988 | antiphospholipid syndrome |
