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S1PR2

sphingosine-1-phosphate receptor 2

HCNC Approved Symbol
S1PR2 (HGNC:3169)
Genomic Coordinates
19:10,221,433 - 10,231,331 (19p13.2)
Synonyms
Gpcr13, H218, AGR16, EDG5, DFNB68
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the S1PR2 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results
S1PR2 - Gene browser | 3billion