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SPNS2

SPNS lysolipid transporter 2, sphingosine-1-phosphate

HCNC Approved Symbol
SPNS2 (HGNC:26992)
Genomic Coordinates
17:4,498,881 - 4,539,035 (17p13.2)
Synonyms
SLC63A2
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Deafness, autosomal recessive 115
618457AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SPNS2 gene.

Frequently observed phenotypes

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

No Results