S1PR2 | ENSG00000267534 | NCBI 9294

Details for: S1PR2

Gene ID: 9294

Symbol: S1PR2

Ensembl ID: ENSG00000267534

Description: sphingosine-1-phosphate receptor 2

Associated with

Class a/1 (rhodopsin-like receptors)
(R-HSA-373076)
G alpha (i) signalling events
(R-HSA-418594)
Gpcr downstream signalling
(R-HSA-388396)
Gpcr ligand binding
(R-HSA-500792)
Lysosphingolipid and lpa receptors
(R-HSA-419408)
Signaling by gpcr
(R-HSA-372790)
Signal transduction
(R-HSA-162582)
Actin cytoskeleton organization
(GO:0030036)
Adenylate cyclase-activating g protein-coupled receptor signaling pathway
(GO:0007189)
Cytoplasm
(GO:0005737)
Excitatory postsynaptic potential
(GO:0060079)
Filopodium assembly
(GO:0046847)
G protein-coupled peptide receptor activity
(GO:0008528)
G protein-coupled receptor activity
(GO:0004930)
G protein-coupled receptor binding
(GO:0001664)
G protein-coupled receptor signaling pathway
(GO:0007186)
Integrin binding
(GO:0005178)
Lipid binding
(GO:0008289)
Negative regulation of excitatory postsynaptic potential
(GO:0090394)
Plasma membrane
(GO:0005886)
Positive regulation of cell population proliferation
(GO:0008284)
Positive regulation of establishment of endothelial barrier
(GO:1903142)
Positive regulation of peptidyl-threonine phosphorylation
(GO:0010800)
Postsynapse
(GO:0098794)
Protein binding
(GO:0005515)
Regulation of metabolic process
(GO:0019222)
Sphingosine-1-phosphate receptor activity
(GO:0038036)
Sphingosine-1-phosphate receptor signaling pathway
(GO:0003376)

Other Information

Proteins

Sphingosine 1-phosphate receptor 2

Genular Protein ID: 1289121696

Symbol: S1PR2_HUMAN

Name: Sphingosine 1-phosphate receptor 2

UniProtKB Accession Codes:

O95136 Q86UN8

Database IDs:

Citations:

PubMed ID: 10617617

Title: Sphingosine 1-phosphate-induced cell proliferation, survival, and related signaling events mediated by G protein-coupled receptors Edg3 and Edg5.

PubMed ID: 10617617

DOI: 10.1074/jbc.275.1.288

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 26805784

Title: Autosomal-recessive hearing impairment due to rare missense variants within S1PR2.

PubMed ID: 26805784

DOI: 10.1016/j.ajhg.2015.12.004

PubMed ID: 29453251

Title: Novel Adipokine, FAM19A5, Inhibits Neointima Formation After Injury Through Sphingosine-1-Phosphate Receptor 2.

PubMed ID: 29453251

DOI: 10.1161/circulationaha.117.032398

Sequence Information:

Length: 353
Mass: 38867
Checksum: 8E37084284ABF7E8
Sequence:

MGSLYSEYLN PNKVQEHYNY TKETLETQET TSRQVASAFI VILCCAIVVE NLLVLIAVAR 
NSKFHSAMYL FLGNLAASDL LAGVAFVANT LLSGSVTLRL TPVQWFAREG SAFITLSASV 
FSLLAIAIER HVAIAKVKLY GSDKSCRMLL LIGASWLISL VLGGLPILGW NCLGHLEACS 
TVLPLYAKHY VLCVVTIFSI ILLAIVALYV RIYCVVRSSH ADMAAPQTLA LLKTVTIVLG 
VFIVCWLPAF SILLLDYACP VHSCPILYKA HYFFAVSTLN SLLNPVIYTW RSRDLRREVL 
RPLQCWRPGV GVQGRRRGGT PGHHLLPLRS SSSLERGMHM PTSPTFLEGN TVV

The gene details are incomplete or unavailable at the moment.

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.

Details for: S1PR2

Associated with

Other Information

Sphingosine 1-phosphate-induced cell proliferation, survival, and related signaling events mediated by G protein-coupled receptors Edg3 and Edg5. PubMed ID: 10617617

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). PubMed ID: 15489334

Autosomal-recessive hearing impairment due to rare missense variants within S1PR2. PubMed ID: 26805784

Novel Adipokine, FAM19A5, Inhibits Neointima Formation After Injury Through Sphingosine-1-Phosphate Receptor 2. PubMed ID: 29453251

Database document:

PubMed ID: 10617617

PubMed ID: 15489334

PubMed ID: 26805784

PubMed ID: 29453251