RGS17 (regulator of G protein signaling 17)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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26575 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Regulator of G protein signaling 17 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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RGS17 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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RGS-17, RGSZ2, hRGS17 |
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Chromosome
Chromosome number
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6 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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6q25.2 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a member of the regulator of G-protein signaling family. This protein contains a conserved, 120 amino acid motif called the RGS domain and a cysteine-rich region. The protein attenuates the signaling activity of G-proteins by binding to |
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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 | Q9UGC6 | ||||||||||
| Protein name | Regulator of G-protein signaling 17 (RGS17) | ||||||||||
| Protein function | Regulates G protein-coupled receptor signaling cascades, including signaling via muscarinic acetylcholine receptor CHRM2 and dopamine receptor DRD2. Inhibits signal transduction by increasing the GTPase activity of G protein alpha subunits, ther | ||||||||||
| PDB | 1ZV4 , 6AM3 | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Predominantly expressed in the cerebellum. Also expressed in the cortex and medulla. Weakly expressed in a number of peripheral tissues notably spleen, lung and leukocytes. {ECO:0000269|PubMed:15096504}. | ||||||||||
| Sequence |
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| Sequence length | 210 | ||||||||||
| 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 categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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