Gene Gene information from NCBI Gene database.
Entrez ID 57030
Gene name Solute carrier family 17 member 7
Gene symbol SLC17A7
Synonyms (NCBI Gene)
BNPIVGLUT1
Chromosome 19
Chromosome location 19q13.33
Summary The protein encoded by this gene is a vesicle-bound, sodium-dependent phosphate transporter that is specifically expressed in the neuron-rich regions of the brain. It is preferentially associated with the membranes of synaptic vesicles and functions in gl
miRNA miRNA information provided by mirtarbase database.
43
miRTarBase ID miRNA Experiments Reference
MIRT017615 hsa-miR-335-5p Microarray 18185580
MIRT1353545 hsa-miR-106a CLIP-seq
MIRT1353546 hsa-miR-106b CLIP-seq
MIRT1353547 hsa-miR-1245 CLIP-seq
MIRT1353548 hsa-miR-1273f CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
76
GO ID Ontology Definition Evidence Reference
GO:0003407 Process Neural retina development IEA
GO:0005254 Function Chloride channel activity IEA
GO:0005254 Function Chloride channel activity ISS
GO:0005313 Function L-glutamate transmembrane transporter activity IBA
GO:0005313 Function L-glutamate transmembrane transporter activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605208 16704 ENSG00000104888
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9P2U7
Protein name Vesicular glutamate transporter 1 (VGluT1) (Brain-specific Na(+)-dependent inorganic phosphate cotransporter) (Solute carrier family 17 member 7)
Protein function Multifunctional transporter that transports L-glutamate as well as multiple ions such as chloride, proton, potassium, sodium and phosphate (PubMed:10820226). At the synaptic vesicle membrane, mainly functions as an uniporter which transports pre
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07690 MFS_1 68 453 Major Facilitator Superfamily Family
Tissue specificity TISSUE SPECIFICITY: Expressed in several regions of the brain including amygdala, cerebellum, cerebral cortex, hippocampus, frontal lobe, medulla, occipital lobe, putamen and temporal lobe. {ECO:0000269|PubMed:10820226}.
Sequence
Sequence length 560
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Synaptic vesicle cycle
Retrograde endocannabinoid signaling
Glutamatergic synapse
Nicotine addiction
  Glutamate Neurotransmitter Release Cycle
Organic anion transporters
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Gastric cancer Likely benign rs145502722 RCV005929547
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 38552733, 39650656
Bipolar Disorder Stimulate 20079890
Cardiomyopathy Hypertrophic Associate 36499607
Colorectal Neoplasms Associate 31612869
Dementia Associate 29343737
Encephalitis Viral Associate 37891420
Gallbladder Neoplasms Associate 40527859
Glioblastoma Inhibit 25749033, 29890994
Glioblastoma Associate 36766715
Glioma Associate 33765507, 36766715