RGS8 (regulator of G protein signaling 8)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 85397 |
| Gene name | Regulator of G protein signaling 8 |
| Gene symbol | RGS8 |
| Synonyms (NCBI Gene) |
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| Chromosome | 1 |
| Chromosome location | 1q25.3 |
| Summary | This gene is a member of the regulator of G protein signaling (RGS) family and encodes a protein with a single RGS domain. Regulator of G protein signaling (RGS) proteins are regulatory and structural components of G protein-coupled receptor complexes. Th |
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miRNA
miRNA information provided by mirtarbase database.
1
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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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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P57771 | ||||||||||
| Protein name | Regulator of G-protein signaling 8 (RGS8) | ||||||||||
| Protein function | Regulates G protein-coupled receptor signaling cascades, including signaling via muscarinic acetylcholine receptor CHRM2 and dopamine receptor DRD2 (By similarity). Inhibits signal transduction by increasing the GTPase activity of G protein alph | ||||||||||
| PDB | 2IHD , 2ODE , 5DO9 | ||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 180 | ||||||||||
| Interactions | View interactions | ||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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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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