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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
cadherin EGF LAG seven-pass G-type receptor 1
Summary
- Gene Symbol
-
- CELSR1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Calcium
- Cell membrane
- Developmental protein
- Disease variant
- Disulfide bond
- EGF-like domain
- G-protein coupled receptor
- Glycoprotein
- Hydroxylation
- Laminin EGF-like domain
- Phosphoprotein
- Reference proteome
- Repeat
- Signal
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q9NYQ6 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| Wnt signaling pathway, planar cell polarity pathway | ||
| central nervous system development | ||
| G protein-coupled receptor signaling pathway | ||
| planar dichotomous subdivision of terminal units involved in lung branching morphogenesis | ||
| neural tube closure |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| membrane | ||
| plasma membrane | ||
| nucleoplasm |
| GO Term | Evidence Code | PMID |
|---|---|---|
| calcium ion binding | ||
| G protein-coupled receptor activity |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- cadherin EGF LAG seven-pass G-type receptor 3
- Functional Category
-
- E: Amino acid transport and metabolism
- G: Carbohydrate transport and metabolism
- M: Cell wall/membrane/envelope biogenesis
| Gene Ontology |
|---|
| calcium ion binding |
| cell surface receptor signaling pathway |
| InterPro |
|---|
| GPCR, family 2-like, 7TM |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050580 | hereditary lymphedema |
Ortholog
| Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 118901615 | BALMU04562 | |||
| 122225267 | PANLE18273 | |||
| 129023052 | 9600_0:00505b |
