P2RY8 (P2Y receptor family member 8)
Gene | |
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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286530 |
Gene name
Gene Name - the full gene name approved by the HGNC.
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P2Y receptor family member 8 |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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P2RY8 |
Synonyms (NCBI Gene)
Gene synonyms aliases
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P2Y8 |
Chromosome
Chromosome number
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X|Y |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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X;Y |
Summary
Summary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene belongs to the family of G-protein coupled receptors, that are preferentially activated by adenosine and uridine nucleotides. This gene is moderately expressed in undifferentiated HL60 cells, and is located on both chromos |
SNPs
SNP information provided by dbSNP.
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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 | Q86VZ1 | ||||||||||
Protein name | S-geranylgeranyl-glutathione receptor P2RY8 (P2Y purinoceptor 8) (P2Y8) | ||||||||||
Protein function | G protein-coupled receptor for S-geranylgeranyl-glutathione (GGG), an endogenous metabolite present in lymphoid tissues. Couples the binding of GGG to the activation of GNA13 and downstream repression of AKT activation in lymphocytes defining th | ||||||||||
Family and domains |
Pfam
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Tissue specificity | TISSUE SPECIFICITY: Barely detectable in normal blood leukocytes. Weaker expression was seen in heart, kidney and lung. Not detected in brain (PubMed:11004484, PubMed:15466006). Expressed in B cells and follicular helper T cells in germinal centers (at pr | ||||||||||
Sequence |
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Sequence length | 359 | ||||||||||
Interactions | View interactions |
Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease information provided by ClinVar, GenCC, and GWAS databases.
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