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MIRAGE
calcium activated nucleotidase 1
Summary
- Gene Symbol
-
- CANT1
- Aliases
-
- SCAN-1
- SHAPY
- Soluble Ca-Activated Nucleotidase, isozyme 1
- apyrase 1 homolog (C. lectularius)
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Calcium
- Cell membrane
- Disease variant
- Disulfide bond
- Dwarfism
- Endoplasmic reticulum
- Glycoprotein
- Golgi apparatus
- Hydrolase
- Metal-binding
- Proteomics identification
- Reference proteome
- Signal-anchor
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q8WVQ1 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| proteoglycan biosynthetic process |
|
|
| proteoglycan biosynthetic process |
|
|
| positive regulation of canonical NF-kappaB signal transduction |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| extracellular region |
|
|
| endoplasmic reticulum membrane |
|
|
| endoplasmic reticulum membrane |
|
|
| Golgi apparatus |
|
|
| plasma membrane |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| GDP phosphatase activity |
|
|
| GDP phosphatase activity |
|
|
| calcium ion binding |
|
|
| calcium ion binding |
|
|
| protein binding |
|
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Soluble calcium-activated nucleotidase
- Functional Category
-
- J: Translation, ribosomal structure and biogenesis
- O: Posttranslational modification, protein turnover, chaperones
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| GDP phosphatase activity |
| UDP phosphatase activity |
| calcium ion binding |
| hydrolase activity |
| nucleoside diphosphate phosphatase activity |
| proteoglycan biosynthetic process |
| InterPro |
|---|
| Apyrase superfamily |
| Apyrase |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060462 | Desbuquois dysplasia | |
| DOID:0070302 | multiple epiphyseal dysplasia 7 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000160 | Narrow mouth |
| HP:0000272 | Malar flattening |
| HP:0000308 | Microretrognathia |
| HP:0000311 | Round face |
| HP:0000319 | Smooth philtrum |
| HP:0000343 | Long philtrum |
| HP:0000368 | Low-set, posteriorly rotated ears |
| HP:0000463 | Anteverted nares |
| HP:0000470 | Short neck |
| Disease ID | Disease Name |
|---|---|
| ORPHA:1425 |
|
| OMIM:617719 |
|
| OMIM:251450 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
