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SLC16A9

Gene

solute carrier family 16 member 9

HGNCHGNC:23520EnsemblENSG00000165449NCBI Gene220963
Locus: gene with protein productLocation: 10q21.2

Also known as

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

Also known asC10orf36 · FLJ43803 · MCT9
View full nomenclature history (8)
Previous symbolsC10orf36
Alias symbolsFLJ43803, MCT9
Previous nameschromosome 10 open reading frame 36, solute carrier family 16 (monocarboxylic acid transporters), member 9, solute carrier family 16, member 9 (monocarboxylic acid transporter 9), solute carrier family 16, member 9
Alias namesmonocarboxylic acid transporter 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.

Gout
Coronary Artery Disease
Temporal arteritis
Placental retention
Alcohol drinking
Smoking initiation
Thyroid Neoplasms

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 16

Provenance

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