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MIRAGE
cadherin, EGF LAG seven-pass G-type receptor 2
Summary
- Gene Symbol
-
- Celsr2
- Organism
- Mus musculus (house mouse)
Annotation
- Keyword
-
- Alternative splicing
- Calcium
- Cell membrane
- Developmental protein
- Direct protein sequencing
- Disulfide bond
- EGF-like domain
- G-protein coupled receptor
- Glycoprotein
- Hydroxylation
- Laminin EGF-like domain
- Reference proteome
- Repeat
- Signal
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q9R0M0 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| cilium movement | ||
| regulation of DNA-templated transcription | ||
| regulation of transcription, DNA-templated | ||
| homophilic cell adhesion via plasma membrane adhesion molecules | ||
| G protein-coupled receptor signaling pathway |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytoplasm | ||
| plasma membrane | ||
| plasma membrane |
| GO Term | Evidence Code | PMID |
|---|---|---|
| G protein-coupled receptor activity | ||
| calcium ion binding | ||
| protein binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Rodentia
- Group Name
- cadherin EGF LAG seven-pass G-type receptor 2
- Functional Category
-
- J: Translation, ribosomal structure and biogenesis
- O: Posttranslational modification, protein turnover, chaperones
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| calcium ion binding |
| cell surface receptor signaling pathway |
| homophilic cell adhesion via plasma membrane adhesion molecules |
| neurogenesis |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:10908 | hydrocephalus |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 1951 | FB:FBgn0024836 | ||
| 1952 | Xenbase:XB-GENE-919957 | HUMAN51116 | |
| 9620 | FB:FBgn0024836 | ||
| 12614 | FB:FBgn0024836 | ||
| 36125 | Xenbase:XB-GENE-919957 | ||
| 53883 | Xenbase:XB-GENE-919957 | ||
| 83465 | RATNO23371 | ||
| 83466 | FB:FBgn0024836 | ||
| 107934 | FB:FBgn0024836 | ||
| 179788 | Xenbase:XB-GENE-919957 |
