Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
53637
Gene name Gene Name - the full gene name approved by the HGNC.
Sphingosine-1-phosphate receptor 5
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
S1PR5
Synonyms (NCBI Gene) Gene synonyms aliases
EDG8, Edg-8, S1P5, SPPR-1, SPPR-2
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19p13.2
Summary Summary of gene provided in NCBI Entrez Gene.
The lysosphingolipid sphingosine 1-phosphate (S1P) regulates cell proliferation, apoptosis, motility, and neurite retraction. Its actions may be both intracellular as a second messenger and extracellular as a receptor ligand. S1P and the structurally rela
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT023008 hsa-miR-124-3p Microarray 18668037
MIRT1324555 hsa-miR-1321 CLIP-seq
MIRT1324556 hsa-miR-133a CLIP-seq
MIRT1324557 hsa-miR-133b CLIP-seq
MIRT1324558 hsa-miR-1915 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003376 Process Sphingosine-1-phosphate receptor signaling pathway IEA
GO:0004930 Function G protein-coupled receptor activity IBA 21873635
GO:0005515 Function Protein binding IPI 32296183
GO:0005737 Component Cytoplasm IBA 21873635
GO:0005886 Component Plasma membrane IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605146 14299 ENSG00000180739
Protein
UniProt ID Q9H228
Protein name Sphingosine 1-phosphate receptor 5 (S1P receptor 5) (S1P5) (Endothelial differentiation G-protein-coupled receptor 8) (Sphingosine 1-phosphate receptor Edg-8) (S1P receptor Edg-8)
Protein function Receptor for the lysosphingolipid sphingosine 1-phosphate (S1P). S1P is a bioactive lysophospholipid that elicits diverse physiological effect on most types of cells and tissues. Is coupled to both the G(i/0)alpha and G(12) subclass of heteromer
PDB 7EW1 , 7YXA
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 53 306 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed in the brain, most prominently in the corpus callosum, which is predominantly white matter. Detected in spleen, peripheral blood leukocytes, placenta, lung, aorta and fetal spleen. Low-level signal detected in many tis
Sequence
Sequence length 398
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Sphingolipid signaling pathway
Neuroactive ligand-receptor interaction
  G alpha (i) signalling events
Lysosphingolipid and LPA receptors
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Inflammatory Bowel Disease Inflammatory Bowel Disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Endometriosis Associate 32907751
Glioblastoma Associate 24903384
Inflammation Inhibit 22715976
Leukemia Associate 18477771
Mouth Diseases Associate 38287231
Mouth Neoplasms Stimulate 34092610
Multiple Sclerosis Associate 32322257
Neoplasms Associate 25084322
Obesity Associate 20950786
Parkinson Disease Associate 34536521