ADGRL3 (adhesion G protein-coupled receptor L3)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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23284 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Adhesion G protein-coupled receptor L3 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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ADGRL3 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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CIRL3, CL3, LEC3, LPHN3 |
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Chromosome
Chromosome number
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4 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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4q13.1 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a member of the latrophilin subfamily of G-protein coupled receptors (GPCR). Latrophilins may function in both cell adhesion and signal transduction. In experiments with non-human species, endogenous proteolytic cleavage within a cystein |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | |||||||||||||||||||||||||||||||||||||||||
| UniProt ID | Q9HAR2 | ||||||||||||||||||||||||||||||||||||||||
| Protein name | Adhesion G protein-coupled receptor L3 (Calcium-independent alpha-latrotoxin receptor 3) (CIRL-3) (Latrophilin-3) (Lectomedin-3) | ||||||||||||||||||||||||||||||||||||||||
| Protein function | Orphan adhesion G-protein coupled receptor (aGPCR), which mediates synapse specificity (PubMed:35418682). Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the | ||||||||||||||||||||||||||||||||||||||||
| PDB | 5CMN , 6VHH , 7SF7 , 8DJG | ||||||||||||||||||||||||||||||||||||||||
| Family and domains |
Pfam
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| Sequence | |||||||||||||||||||||||||||||||||||||||||
| Sequence length | 1447 | ||||||||||||||||||||||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||||||||||||||||||||||
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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