Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
286530
Gene name Gene Name - the full gene name approved by the HGNC.
P2Y receptor family member 8
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
P2RY8
Synonyms (NCBI Gene) Gene synonyms aliases
P2Y8
Chromosome Chromosome number
X|Y
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
X;Y
Summary Summary of gene provided in NCBI Entrez Gene.
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.
SNP ID Visualize variation Clinical significance Consequence
rs1603452612 G>C Likely-pathogenic Coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1209103 hsa-miR-103a CLIP-seq
MIRT1209104 hsa-miR-107 CLIP-seq
MIRT1209105 hsa-miR-3150b-3p CLIP-seq
MIRT1209106 hsa-miR-324-5p CLIP-seq
MIRT1209107 hsa-miR-331-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IBA 21873635
GO:0005887 Component Integral component of plasma membrane IBA 21873635
GO:0035025 Process Positive regulation of Rho protein signal transduction IBA 21873635
GO:0035589 Process G protein-coupled purinergic nucleotide receptor signaling pathway IEA
GO:0045028 Function G protein-coupled purinergic nucleotide receptor activity IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
300525 15524 ENSG00000182162
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

Accession ID Position in sequence Description Type
PF00001 7tm_1 40 293 7 transmembrane receptor (rhodopsin family) Family
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
Sequence length 359
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Neuroactive ligand-receptor interaction  
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Lymphoblastic leukemia Childhood Acute Lymphoblastic Leukemia, L2 Acute Lymphoblastic Leukemia, Precursor Cell Lymphoblastic Leukemia Lymphoma rs387906351, rs104894562, rs398122513, rs398122840, rs1057524466, rs1064796115, rs1064795660, rs1064793129, rs1064796227, rs1567887558, rs1161194345, rs1597558200, rs1406320425, rs1597566470, rs1597566699
View all (13 more)
19838194
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Renal Cell Associate 36360294
Celiac Disease Stimulate 40650227
Crohn Disease Stimulate 40650227
Hirschsprung disease type d brachydactyly Associate 21106984
Inflammation Associate 40650227
Klinefelter Syndrome Associate 32959501
Leukemia Biphenotypic Acute Associate 20378752
Lupus Erythematosus Systemic Associate 34901992
Lymphoma Follicular Associate 27959929
Lymphoma Large B Cell Diffuse Associate 22343534