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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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MIRAGE
calcium sensing receptor
Summary
- Gene Symbol
-
- CASR
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Calcium
- Cell membrane
- Disease variant
- Disulfide bond
- Epilepsy
- G-protein coupled receptor
- Glycoprotein
- Metal-binding
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Signal
- Transmembrane helix
- Ubl conjugation
- Proteins
| UniProt | Protein Name |
|---|---|
| P41180 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| JNK cascade | ||
| chemosensory behavior | ||
| positive regulation of cell population proliferation | ||
| anatomical structure morphogenesis | ||
| positive regulation of gene expression |
GO Hierarchy
biological process
cellular process [inference]
response to stimulus [inference]
localization [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of metabolic process [inference]
regulation of signaling [inference]
regulation of localization [inference]
positive regulation of biological process [inference]
regulation of response to stimulus [inference]
regulation of cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| plasma membrane | ||
| plasma membrane | ||
| plasma membrane | ||
| cell surface | ||
| basolateral plasma membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| phosphatidylinositol phospholipase C activity | ||
| G protein-coupled receptor activity | ||
| G protein-coupled receptor activity | ||
| integrin binding | ||
| calcium ion binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- metabotropic glutamate receptor
- Functional Category
-
- E: Amino acid transport and metabolism
- M: Cell wall/membrane/envelope biogenesis
- T: Signal transduction mechanisms
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060700 | familial hypocalciuric hypercalcemia 1 | |
| DOID:0080652 | calcium oxalate nephrolithiasis | |
| DOID:0090107 | autosomal dominant hypocalcemia 1 | |
| DOID:0090109 | autosomal dominant hypocalcemia | |
| DOID:0111322 | obsolete idiopathic generalized epilepsy 8 | |
| DOID:1059 | intellectual disability | |
| DOID:12466 | secondary hyperparathyroidism | |
| DOID:12678 | hypercalcemia | |
| DOID:13543 | hyperparathyroidism | |
| DOID:585 | nephrolithiasis |
