GPR45 (G protein-coupled receptor 45)
| Gene | |
|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
11250 |
|
Gene name
Gene Name - the full gene name approved by the HGNC.
|
G protein-coupled receptor 45 |
|
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
|
GPR45 |
|
Synonyms (NCBI Gene)
Gene synonyms aliases
|
PSP24, PSP24(ALPHA), PSP24-1, PSP24-alpha, PSP24A |
|
Chromosome
Chromosome number
|
2 |
|
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
2q12.1 |
|
Summary
Summary of gene provided in NCBI Entrez Gene.
|
This intronless gene encodes a member of the G protein-coupled receptor (GPCR) family. Members of this protein family contain seven putative transmembrane domains and may mediate signaling processes to the interior of the cell via activation of heterotrim |
|
miRNA
miRNA information provided by mirtarbase database.
|
|||||||||||||||||||||||||
|
|||||||||||||||||||||||||
|
Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
|
|||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||
|
Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
|
|||||||
|
|||||||
| Protein | |||||||||||
| UniProt ID | Q9Y5Y3 | ||||||||||
| Protein name | Probable G-protein coupled receptor 45 (PSP24-1) (PSP24-alpha) | ||||||||||
| Protein function | Orphan receptor. May play a role in brain function. | ||||||||||
| Family and domains |
Pfam
|
||||||||||
| Tissue specificity | TISSUE SPECIFICITY: Expressed in brain; detected in the basal forebrain, frontal cortex, and caudate, but not in thalamus, hippocampus, or putamen. | ||||||||||
| Sequence |
|
||||||||||
| Sequence length | 372 | ||||||||||
| Interactions | View interactions | ||||||||||
|
Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
|
|||||||
|
|||||||
|
Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
|
|||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||