| Gene Symbol | S1PR2 |
| Entrez Gene ID | 9294 |
| Full Name | sphingosine-1-phosphate receptor 2 |
| Synonyms | AGR16,DFNB68,EDG-5,EDG5,Gpcr13,H218,LPB2,S1P2 |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | This gene encodes a member of the G protein-coupled receptors, as well as the EDG family of proteins. The encoded protein is a receptor for sphingosine 1-phosphate, which participates in cell proliferation, survival, and transcriptional activation. Defects in this gene have been associated with congenital profound deafness. [provided by RefSeq, Mar 2016]. |
| Disorder MIM: | |
| Disorder Html: | Deafness, autosomal recessive 68, 610419 (3) |

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