Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
124976
Gene name Gene Name - the full gene name approved by the HGNC.
SPNS lysolipid transporter 2, sphingosine-1-phosphate
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SPNS2
Synonyms (NCBI Gene) Gene synonyms aliases
DFNB115, SLC62A2, SLC63A2
Disease Acronyms (UniProt) Disease acronyms from UniProt database
DFNB115
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17p13.2
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a transporter of sphingosine 1-phosphate, a secreted lipid that is important in cardiovascular, immunological, and neural development. Defects in this gene are a cause of early onset progressive hearing loss. [provided
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs749994718 TCC>- Pathogenic, uncertain-significance Coding sequence variant, inframe deletion
rs1555537637 CC>T Likely-pathogenic, pathogenic Frameshift variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018966 hsa-miR-335-5p Microarray 18185580
MIRT647400 hsa-miR-8485 HITS-CLIP 23824327
MIRT647401 hsa-miR-7113-5p HITS-CLIP 23824327
MIRT647399 hsa-miR-4685-5p HITS-CLIP 23824327
MIRT647398 hsa-miR-6837-5p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001782 Process B cell homeostasis IEA
GO:0002920 Process Regulation of humoral immune response IEA
GO:0003376 Process Sphingosine-1-phosphate receptor signaling pathway IEA
GO:0005886 Component Plasma membrane IEA
GO:0006665 Process Sphingolipid metabolic process IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
612584 26992 ENSG00000183018
Protein
UniProt ID Q8IVW8
Protein name Sphingosine-1-phosphate transporter SPNS2 (Protein spinster homolog 2)
Protein function Lipid transporter that specifically mediates export of sphingosine-1-phosphate (sphing-4-enine 1-phosphate, S1P) and sphinganine-1-phosphate in the lymph, thereby playing a role in lymphocyte trafficking (PubMed:19074308, PubMed:21084291, PubMed
PDB 7YUB , 7YUD , 7YUF , 8EX4 , 8EX5 , 8EX6 , 8EX7 , 8EX8 , 8G92 , 8JHQ , 8JHR , 8KAE , 8QV5 , 8QV6 , 8RL7 , 8RL8 , 8RLC , 8RLD
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07690 MFS_1 108 476 Major Facilitator Superfamily Family
Sequence
Sequence length 549
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Hearing loss Sensorineural Hearing Loss (disorder) rs267607135, rs267606855, rs779841884, rs267606854, rs28942097, rs121908073, rs121908076, rs74315289, rs121908144, rs111033313, rs74315437, rs121908348, rs121908349, rs121908350, rs397515359
View all (184 more)
Multiple congenital anomalies Multiple congenital anomalies rs1057517732 27899622, 19074308, 25356849
Unknown
Disease term Disease name Evidence References Source
Deafness hearing loss, autosomal recessive 115 GenCC
Associations from Text Mining
Disease Name Relationship Type References
Fibrosis Associate 29772789
Glioblastoma Inhibit 37728571
Glioma Inhibit 37728571
Inflammation Associate 29772789
Liver Failure Associate 27562371
Lymphatic Metastasis Associate 33673355
Lymphatic Metastasis Inhibit 34092610
Mouth Neoplasms Associate 34092610
Neoplasms Associate 36057880
Neoplasms Inhibit 37728571