GPR85 (G protein-coupled receptor 85)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 54329 |
| Gene name | G protein-coupled receptor 85 |
| Gene symbol | GPR85 |
| Synonyms (NCBI Gene) |
SREBSREB2
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| Chromosome | 7 |
| Chromosome location | 7q31.1 |
| Summary | Members of the G protein-coupled receptor (GPCR) family, such as GPR85, have a similar structure characterized by 7 transmembrane domains. Activation of GPCRs by extracellular stimuli, such as neurotransmitters, hormones, or light, induces an intracellula |
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miRNA
miRNA information provided by mirtarbase database.
83
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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P60893 | ||||||||||
| Protein name | Probable G-protein coupled receptor 85 (Super conserved receptor expressed in brain 2) | ||||||||||
| Protein function | Orphan receptor. | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Highly expressed in brain and testis. Lower levels in small intestine, placenta and spleen. In brain regions, detected in all regions tested, but somewhat lower levels in the corpus callosum, medulla and spinal cord. {ECO:0000269|PubMe | ||||||||||
| Sequence | |||||||||||
| Sequence length | 370 | ||||||||||
| Interactions | View interactions | ||||||||||
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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