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annexin A5
Summary
- Gene Symbol
-
- ANXA5
- Aliases
-
- CPB-I
- Calphobindin I
- PAP-I
- Placental anticoagulant protein I
- RPRGL3
- VAC-alph
- Vascular anticoagulant-alpha
- annexin V
- endonexin II
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Annexin
- Blood coagulation
- Calcium/phospholipid-binding
- Direct protein sequencing
- Isopeptide bond
- Phosphoprotein
- Reference proteome
- Repeat
- S-nitrosylation
- Ubl conjugation
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| negative regulation of apoptotic process |
|
|
| response to organic substance | ||
| negative regulation of coagulation | ||
| signal transduction |
|
|
| blood coagulation |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytosol |
|
|
| extracellular region |
|
|
| cytoplasm | ||
| external side of plasma membrane | ||
| vesicle membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| calcium-dependent phospholipid binding | ||
| phosphatidylserine binding | ||
| phospholipase inhibitor activity |
|
|
| calcium ion binding | ||
| phospholipid binding |
|
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080348 | Alzheimer's disease 1 | |
| DOID:0080379 | nephrotic syndrome type 2 | |
| DOID:0080409 | familial adenomatous polyposis 1 | |
| DOID:0090016 | chromosome 5q deletion syndrome | |
| DOID:0090110 | immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | |
| DOID:0090119 | ankyloblepharon-ectodermal defects-cleft lip/palate syndrome | |
| DOID:0110035 | Alzheimer's disease 2 | |
| DOID:0110037 | Alzheimer's disease 5 | |
| DOID:0110038 | Alzheimer's disease 6 | |
| DOID:0110039 | Alzheimer's disease 7 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0011462 | Young adult onset |
| Disease ID | Disease Name |
|---|---|
| OMIM:614391 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 115540458 | GADMO41489 | ||
| 100049533 | ORYLA00491 | ||
| 100534399 | ORENI62675 | ||
| 115589710 | SPAAU57364 | ||
| 398472 | Xenbase:XB-GENE-1007301 | ||
| 443760 | Xenbase:XB-GENE-17346866 | ||
| 493545 | Xenbase:XB-GENE-1007295 | ||
| 101942442 | CHRPI11594 | ||
| 109309325 | CROPO16843 | ||
| 113434697 | PSETE05431 |
