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SLC17A7

Gene

solute carrier family 17 member 7

HGNCHGNC:16704EnsemblENSG00000104888NCBI Gene57030
Locus: gene with protein productLocation: 19q13.33

Encodes

via encodes

The protein product this gene encodes, reached through the canonical GENE→PROTEIN (encodes) relation. Its biology, drugs, indications, trials and therapeutic evidence live on the protein's own page.

Vesicular glutamate transporter 1Q9P2U7

Protein · therapeutic target

Explore protein biology & therapeutics

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asBNPI · VGLUT1
View full nomenclature history (5)
Alias symbolsBNPI, VGLUT1
Previous namessolute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 7, solute carrier family 17 (vesicular glutamate transporter), member 7
Alias namesvesicular glutamate transporter 1

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Parkinson's Disease
Genetic developmental and epileptic encephalopathy
Fragile X Syndrome
Autistic Disorder
Undetermined early-onset epileptic encephalopathy
Alzheimer's Disease
Glioblastoma

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Solute carrier family 17

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.