P2RY11 - purinergic receptor P2Y11 Gene

Also Known as P2Y11

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 5032

About P2RY11

Cytogenetic location: 19p13.2 Genomic coordinates (GRCh38): 19:10,111,693-10,115,372 (from NCBI)

This gene has 2 transcripts (splice variants), 145 orthologues, 7 paralogues and is associated with 1 phenotype. Ubiquitous expression in spleen (RPKM 6.0), lymph node (RPKM 4.7) and 25 other tissues.

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 is coupled to the stimulation of the phosphoinositide and adenylyl cyclase pathways and behaves as a selective purinoceptor. Naturally occuring read-through transcripts, resulting from intergenic splicing between this gene and an immediately upstream gene (PPAN, encoding peter pan homolog), have been found. The PPAN-P2RY11 read-through mRNA is ubiquitously expressed and encodes a fusion protein that shares identity with each individual gene product. [provided by RefSeq, Jul 2008]

P2RY11 Products (1)

mRNA Protein Name
NM_002566.5 NP_002557.2 P2Y purinoceptor 11
Molecular Function GO Annotation Evidence Références Source
enables G protein-coupled ATP receptor activity IDA
IDA: Inferred from direct assay
18048695 GOA
enables neurotransmitter receptor activity IDA
IDA: Inferred from direct assay
18048695 GOA
Biological Process GO Annotation Evidence Références Source
involved in G protein-coupled receptor signaling pathway IDA
IDA: Inferred from direct assay
18048695 GOA
involved in calcium-mediated signaling IDA
IDA: Inferred from direct assay
18048695 GOA
involved in cellular response to ATP IDA
IDA: Inferred from direct assay
18048695 GOA
involved in neuronal signal transduction IDA
IDA: Inferred from direct assay
18048695 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

P2RY11 Protein Structure

7tm_1

7tm_1: 7 transmembrane receptor (rhodopsin family) (46 - 277)

  • 0
  • 100
  • 200
  • 300
  • 374 a.a.
Protein Preferred Names Protein Names

P2Y purinoceptor 11

  • purinergic receptor P2Y, G-protein coupled, 11

Related Diseases

Diseases Alias
Recurrent Hypersomnia
  • Primary Recurrent Hypersomnia

  • Hypersomnia Recurrent

  • Disorders Of Excessive Somnolence

  • Hypersomnia, Recurrent

Narcolepsy 1
  • NRCLP1

  • Narcoleptic Syndrome 1

  • Gelineau Disease

  • Narcolepsy-Cataplexy

  • Narcolepsy-Cataplexy Syndrome

  • Narcolepsy, Type 1

  • Narcolepsy Type 1

  • Cataplexy

  • Gélineau'S Syndrome

  • Narcolepsy With Cataplexy And/Or Hypocretin Deficiency

Narcolepsy
  • Paroxysmal Sleep

  • Gelineau Syndrome

  • Narcoleptic Syndrome

  • Narcolepsy-Cataplexy Syndrome

  • Cataplexy And Narcolepsy

  • Narcolepsy, Without Cataplexy

  • Gelineau'S Syndrome

  • Narcolepsy With Or Without Cataplexy

  • Narcolepsy Nos

Kleine-Levin Hibernation Syndrome
  • Kleine-Levin Syndrome

  • Familial Kleine-Levin Syndrome

  • Kleine Levin Syndrome

  • Familial Hibernation Syndrome

  • Recurrent Hypersomnolence

  • Hypersomnia-Bulimia Syndrome

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus P2RY11 VGNC VGNC:106855
Canis familiaris P2RY11 VGNC VGNC:108251
Rattus norvegicus P2RY11 RGD RGD:7666983
Others P2RY11 NCBI