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SLC17A9

Gene

solute carrier family 17 member 9

HGNCHGNC:16192EnsemblENSG00000101194NCBI Gene63910
Locus: gene with protein productLocation: 20q13.33

Also known as

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

Also known asC20orf59 · FLJ23412 · VNUT
View full nomenclature history (6)
Previous symbolsC20orf59
Alias symbolsFLJ23412, VNUT
Previous nameschromosome 20 open reading frame 59, solute carrier family 17, member 9, solute carrier family 17 (vesicular nucleotide transporter), member 9

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.

Disseminated superficial actinic porokeratosis
Carcinoma, Hepatocellular
Neoplasms
hyperinsulinism due to INSR deficiency

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.