Gene Gene information from NCBI Gene database.
Entrez ID 201305
Gene name SPNS lysolipid transporter 3, sphingosine-1-phosphate (putative)
Gene symbol SPNS3
Synonyms (NCBI Gene)
SLC62A3SLC63A3
Chromosome 17
Chromosome location 17p13.2
miRNA miRNA information provided by mirtarbase database.
10
miRTarBase ID miRNA Experiments Reference
MIRT1385056 hsa-miR-3144-5p CLIP-seq
MIRT1385057 hsa-miR-3151 CLIP-seq
MIRT1385058 hsa-miR-3188 CLIP-seq
MIRT1385059 hsa-miR-3191 CLIP-seq
MIRT1385060 hsa-miR-4327 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183, 33961781
GO:0006869 Process Lipid transport IEA
GO:0016020 Component Membrane IBA
GO:0016020 Component Membrane IEA
GO:0022857 Function Transmembrane transporter activity IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611701 28433 ENSG00000182557
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6ZMD2
Protein name Protein spinster homolog 3
Protein function Sphingolipid transporter.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07690 MFS_1 51 420 Major Facilitator Superfamily Family
Sequence
Sequence length 512
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
CLONAL HEMATOPOIESIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CORONARY ARTERY DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PSYCHIATRIC DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SCHIZOPHRENIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Colorectal Neoplasms Associate 24349560
★☆☆☆☆
Found in Text Mining only
Leukemia Myeloid Acute Associate 34608834, 35249471
★☆☆☆☆
Found in Text Mining only