Gene: S1PR2

Alternate names for this Gene: AGR16|DFNB68|EDG-5|EDG5|Gpcr13|H218|LPB2|S1P2

Gene 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.

Gene is located in Chromosome: 19

Location in Chromosome : 19p13.2

Description of this Gene: sphingosine-1-phosphate receptor 2

Type of Gene: protein-coding