Gene Gene information from NCBI Gene database.
Entrez ID 5032
Gene name Purinergic receptor P2Y11
Gene symbol P2RY11
Synonyms (NCBI Gene)
P2Y11
Chromosome 19
Chromosome location 19p13.2
Summary The product of this gene belongs to the family of G-protein coupled receptors. This family has several receptor subtypes with different pharmacological selectivity, which overlaps in some cases, for various adenosine and uridine nucleotides. This receptor
miRNA miRNA information provided by mirtarbase database.
105
miRTarBase ID miRNA Experiments Reference
MIRT048698 hsa-miR-99a-5p CLASH 23622248
MIRT1208994 hsa-miR-1247 CLIP-seq
MIRT1208995 hsa-miR-1273 CLIP-seq
MIRT1208996 hsa-miR-1275 CLIP-seq
MIRT1208997 hsa-miR-23a CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
26
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IC 18048695
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane TAS 9405388
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
602697 8540 ENSG00000244165
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96G91
Protein name P2Y purinoceptor 11 (P2Y11)
Protein function Receptor for ATP and ADP coupled to G-proteins that activate both phosphatidylinositol-calcium and adenylyl cyclase second messenger systems. Not activated by UTP or UDP.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 45 297 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Highest expression in liver and spleen. {ECO:0000269|PubMed:11278528}.
Sequence
Sequence length 374
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Neuroactive ligand-receptor interaction   G alpha (q) signalling events
P2Y receptors
G alpha (s) signalling events
ADORA2B mediated anti-inflammatory cytokines production
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
8
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cataplexy and narcolepsy association rs12460842, rs2305795 RCV000161131
RCV000161132
P2RY11-related disorder Likely benign; Benign rs774978141, rs753346854, rs112371201, rs139489816, rs3745601, rs111752629 RCV003909260
RCV003901826
RCV003942035
RCV003943945
RCV003981999
RCV003930743
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Autoimmune Diseases Associate 21170044
Carcinoma Squamous Cell Associate 18057535
Colorectal Neoplasms Associate 34768902
Demyelinating Autoimmune Diseases CNS Associate 24524250
Diabetes Mellitus Type 2 Associate 30592156
Hypoxia Inhibit 26433470
Inflammation Associate 36107259
Lung Neoplasms Associate 26491047
Myocardial Infarction Associate 37798364
Myoclonus Associate 33710305