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 (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
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)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
Cataplexy and narcolepsy association ClinVar
Disgenet
★★★☆☆
Reported in Unknown/Other Associations (≥2 sources)
NARCOLEPSY CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
NARCOLEPSY TYPE 1 Disgenet, Orphanet
Disgenet, Orphanet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
P2RY11-related disorder Likely benign; Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations