P2RY12

GENERAL INFORMATION

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Gene name

P2RY12

Gene description

Purinergic receptor P2Y, G-protein coupled, 12

Protein class

Disease related genes
FDA approved drug targets
G-protein coupled receptors
Predicted membrane proteins

Predicted localization

Membrane

Number of transcripts

1
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (cerebral cortex)
GTEx:Tissue enhanced (cerebral cortex, hippocampus)

Protein evidence

Evidence at protein level

Protein localization

Selective cytoplasmic and nuclear expression in microglia as well as subsets of cells in bone marrow and lymphoid tissues.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining consistent with RNA expression data.

Data reliability

Supportive based on 2 antibodies.
HPA013796 , HPA014518
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Bone marrow

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (cerebral cortex)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (cerebral cortex, hippocampus)

Organ

Expression



GENE INFORMATION

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Gene name

P2RY12 (HGNC Symbol)

Synonyms

HORK3, P2Y12, SP1999

Description

Purinergic receptor P2Y, G-protein coupled, 12 (HGNC Symbol)

Entrez gene 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 involved in platelet aggregation, and is a potential target for the treatment of thromboembolisms and other clotting disorders. Mutations in this gene are implicated in bleeding disorder, platelet type 8 (BDPLT8). Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]

Chromosome

3

Cytoband

q25.1

Chromosome location (bp)

151337380 - 151384812

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000169313 (version 78.38)

Entrez gene

64805

UniProt

Q9H244 (UniProt - Evidence at protein level)

neXtProt

NX_Q9H244

Antibodypedia

P2RY12 antibodies


PROTEIN BROWSER

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ENST00000302632
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

P2RY12-001 ENSP00000307259
ENST00000302632
Q9H244
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