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SLC9A4

Gene

solute carrier family 9 member A4

HGNCHGNC:11077EnsemblENSG00000180251NCBI Gene389015
Locus: gene with protein productLocation: 2q12.1

Also known as

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

Also known asNHE4
View full nomenclature history (4)
Alias symbolsNHE4
Previous namessolute carrier family 9 (sodium/hydrogen exchanger), isoform 4, solute carrier family 9 (sodium/hydrogen exchanger), member 4, solute carrier family 9, subfamily A (NHE4, cation proton antiporter 4), member 4

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.

Asthma
Inflammatory Bowel Diseases
Crohn's Disease
Dermatitis, Atopic
Sleep Apnea, Obstructive
Leprosy
Sleep Apnea Syndromes
Chronic rhinosinusitis
Sleep disorder

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 9

Provenance

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