The S1PR2 gene homepage

General information
Gene symbol S1PR2
Gene name sphingosine-1-phosphate receptor 2
Chromosome 19
Chromosomal band q13
Imprinted Unknown
Genomic reference NG_046802.1
Transcript reference NM_004230.3
Exon/intron information NM_004230.3 exon/intron table
Associated with diseases DFNB, DFNB68
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Barbara Vona
Total number of public variants reported 10
Unique public DNA variants reported 10
Individuals with public variants 54
Hidden variants -
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 03, 2013
Date last updated May 09, 2022
Version S1PR2:220509

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_004230.3.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/S1PR2
HGNC 3169
Entrez Gene 9294
PubMed articles S1PR2
OMIM - Gene 605111
OMIM - Diseases DFNB68 (deafness, autosomal recessive, type 68 (DFNB-68))
HGMD S1PR2
GeneCards S1PR2
GeneTests S1PR2
Orphanet S1PR2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00018337 19 sphingosine-1-phosphate receptor 2 NM_004230.3 NP_004221.3 10


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