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SLC9A9

Gene

solute carrier family 9 member A9

HGNCHGNC:20653EnsemblENSG00000181804NCBI Gene285195
Locus: gene with protein productLocation: 3q24

Also known as

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

Also known asFLJ35613 · NHE9
View full nomenclature history (5)
Alias symbolsFLJ35613, NHE9
Previous namessolute carrier family 9 (sodium/hydrogen exchanger), member 9, solute carrier family 9 (sodium/hydrogen exchanger), isoform 9, solute carrier family 9, subfamily A (NHE9, cation proton antiporter 9), 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.

Autistic Disorder
Iron Metabolism Disorders
Chondrocalcinosis
Ovarian neoplasm
Corneal Ulcer

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.